Canonical Allele Identifier: CA2429757382
Gene: KDM5C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.53194904_53194905delinsCT , CM000685.2:g.53194904_53194905delinsCT GRCh38
NC_000023.10:g.53224086_53224087delinsCT , CM000685.1:g.53224086_53224087delinsCT GRCh37
NC_000023.9:g.53240811_53240812delinsCT NCBI36
NG_008085.1:g.35518_35519delinsAG
NG_008085.2:g.35518_35519delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000685423.1:c.3438+26_3438+27delinsAG ENSP00000508806.1:n.3438+26_3438+27delinsAG
ENST00000685641.1:c.3438+26_3438+27delinsAG ENSP00000509818.1:n.3438+26_3438+27delinsAG
ENST00000687695.1:c.3435+26_3435+27delinsAG ENSP00000508631.1:n.3435+26_3435+27delinsAG
ENST00000688699.1:c.3438+26_3438+27delinsAG ENSP00000510430.1:n.3438+26_3438+27delinsAG
ENST00000691505.1:c.3438+26_3438+27delinsAG ENSP00000510354.1:n.3438+26_3438+27delinsAG
ENST00000693277.1:c.2943+26_2943+27delinsAG ENSP00000510522.1:n.2943+26_2943+27delinsAG
ENST00000375401.8:c.3438+26_3438+27delinsAG MANE Select ENSP00000364550.4:n.3438+26_3438+27delinsAG
ENST00000375379.7:c.3438+26_3438+27delinsAG ENSP00000364528.3:n.3438+26_3438+27delinsAG
ENST00000375383.7:c.3315+26_3315+27delinsAG ENSP00000364532.3:n.3315+26_3315+27delinsAG
ENST00000375401.7:c.3438+26_3438+27delinsAG ENSP00000364550.3:n.3438+26_3438+27delinsAG
ENST00000404049.7:c.3435+26_3435+27delinsAG ENSP00000385394.3:n.3435+26_3435+27delinsAG
ENST00000452825.7:c.3237+26_3237+27delinsAG ENSP00000445176.1:n.3237+26_3237+27delinsAG
NM_001146702.1:c.3237+26_3237+27delinsAG NP_001140174.1:n.3237+26_3237+27delinsAG
NM_001282622.1:c.3435+26_3435+27delinsAG NP_001269551.1:n.3435+26_3435+27delinsAG
NM_004187.3:c.3438+26_3438+27delinsAG NP_004178.2:n.3438+26_3438+27delinsAG
XM_005262035.3:c.3438+26_3438+27delinsAG XP_005262092.1:n.3438+26_3438+27delinsAG
XM_006724609.2:c.3438+26_3438+27delinsAG XP_006724672.1:n.3438+26_3438+27delinsAG
XM_011530824.1:c.3360+26_3360+27delinsAG XP_011529126.1:n.3360+26_3360+27delinsAG
XM_011530825.1:c.3315+26_3315+27delinsAG XP_011529127.1:n.3315+26_3315+27delinsAG
XM_011530826.1:c.3315+26_3315+27delinsAG XP_011529128.1:n.3315+26_3315+27delinsAG
XM_011530827.1:c.3438+26_3438+27delinsAG XP_011529129.1:n.3438+26_3438+27delinsAG
XM_011530828.1:c.3438+26_3438+27delinsAG XP_011529130.1:n.3438+26_3438+27delinsAG
XM_011530829.1:c.2943+26_2943+27delinsAG XP_011529131.1:n.2943+26_2943+27delinsAG
XM_011530830.1:c.2943+26_2943+27delinsAG XP_011529132.1:n.2943+26_2943+27delinsAG
XM_011530831.1:c.2454+26_2454+27delinsAG XP_011529133.1:n.2454+26_2454+27delinsAG
XR_938369.1:n.3784+26_3784+27delinsAG
XR_938370.1:n.3784+26_3784+27delinsAG
XR_938371.1:n.3784+26_3784+27delinsAG
XR_938372.1:n.3784+26_3784+27delinsAG
XR_938373.1:n.3784+26_3784+27delinsAG
NM_001353978.1:c.3438+26_3438+27delinsAG NP_001340907.1:n.3438+26_3438+27delinsAG
NM_001353979.1:c.3435+26_3435+27delinsAG NP_001340908.1:n.3435+26_3435+27delinsAG
NM_001353981.1:c.3438+26_3438+27delinsAG NP_001340910.1:n.3438+26_3438+27delinsAG
NM_001353982.1:c.3435+26_3435+27delinsAG NP_001340911.1:n.3435+26_3435+27delinsAG
NM_001353984.1:c.3438+26_3438+27delinsAG NP_001340913.1:n.3438+26_3438+27delinsAG
NR_148672.1:n.3971+26_3971+27delinsAG
NR_148673.1:n.3968+26_3968+27delinsAG
NR_148674.1:n.3848+26_3848+27delinsAG
XM_011530824.3:c.3360+26_3360+27delinsAG XP_011529126.1:n.3360+26_3360+27delinsAG
XM_011530825.3:c.3315+26_3315+27delinsAG XP_011529127.1:n.3315+26_3315+27delinsAG
XM_011530826.3:c.3315+26_3315+27delinsAG XP_011529128.1:n.3315+26_3315+27delinsAG
XM_011530827.3:c.3438+26_3438+27delinsAG XP_011529129.1:n.3438+26_3438+27delinsAG
XM_011530828.2:c.3438+26_3438+27delinsAG XP_011529130.1:n.3438+26_3438+27delinsAG
XM_011530829.2:c.2943+26_2943+27delinsAG XP_011529131.1:n.2943+26_2943+27delinsAG
XM_011530830.2:c.2943+26_2943+27delinsAG XP_011529132.1:n.2943+26_2943+27delinsAG
XM_011530831.2:c.2454+26_2454+27delinsAG XP_011529133.1:n.2454+26_2454+27delinsAG
XM_024452466.1:c.3435+26_3435+27delinsAG XP_024308234.1:n.3435+26_3435+27delinsAG
XR_001755735.2:n.3764+26_3764+27delinsAG
XR_001755736.2:n.3764+26_3764+27delinsAG
XR_001755737.2:n.3764+26_3764+27delinsAG
XR_938370.3:n.3764+26_3764+27delinsAG
NM_001146702.2:c.3237+26_3237+27delinsAG NP_001140174.1:n.3237+26_3237+27delinsAG
NM_001282622.3:c.3435+26_3435+27delinsAG NP_001269551.1:n.3435+26_3435+27delinsAG
NM_001353978.3:c.3438+26_3438+27delinsAG NP_001340907.1:n.3438+26_3438+27delinsAG
NM_001353979.2:c.3435+26_3435+27delinsAG NP_001340908.1:n.3435+26_3435+27delinsAG
NM_001353981.2:c.3438+26_3438+27delinsAG NP_001340910.1:n.3438+26_3438+27delinsAG
NM_001353982.2:c.3435+26_3435+27delinsAG NP_001340911.1:n.3435+26_3435+27delinsAG
NM_004187.5:c.3438+26_3438+27delinsAG MANE Select NP_004178.2:n.3438+26_3438+27delinsAG
NR_148672.2:n.3756+26_3756+27delinsAG
NR_148673.2:n.3753+26_3753+27delinsAG
NR_148674.2:n.3633+26_3633+27delinsAG
NM_001353984.2:c.3438+26_3438+27delinsAG NP_001340913.1:n.3438+26_3438+27delinsAG