Canonical Allele Identifier: CA413133412

Gene: KDM5C

Linked Data

• MyVariant Identifiers: chrX:g.53245285A>C (hg19) ; chrX:g.53216103A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53216103A>C , CM000685.2:g.53216103A>C	GRCh38
NC_000023.10:g.53245285A>C , CM000685.1:g.53245285A>C	GRCh37
NC_000023.9:g.53262010A>C	NCBI36
NG_008085.1:g.14320T>G
NG_008085.2:g.14320T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465402.2:n.1083T>G
ENST00000685423.1:c.752T>G	ENSP00000508806.1:p.Met251Arg
ENST00000685539.1:n.1096T>G
ENST00000685641.1:c.752T>G	ENSP00000509818.1:p.Met251Arg
ENST00000687695.1:c.749T>G	ENSP00000508631.1:p.Met250Arg
ENST00000687928.1:n.1022T>G
ENST00000688699.1:c.752T>G	ENSP00000510430.1:p.Met251Arg
ENST00000691505.1:c.752T>G	ENSP00000510354.1:p.Met251Arg
ENST00000693277.1:c.257T>G	ENSP00000510522.1:p.Met86Arg
ENST00000375401.8:c.752T>G MANE Select	ENSP00000364550.4:p.Met251Arg
ENST00000375379.7:c.752T>G	ENSP00000364528.3:p.Met251Arg
ENST00000375383.7:c.629T>G	ENSP00000364532.3:p.Met210Arg
ENST00000375401.7:c.752T>G	ENSP00000364550.3:p.Met251Arg
ENST00000404049.7:c.749T>G	ENSP00000385394.3:p.Met250Arg
ENST00000452825.7:c.551T>G	ENSP00000445176.1:p.Met184Arg
ENST00000497995.1:n.102T>G
NM_001146702.1:c.551T>G	NP_001140174.1:p.Met184Arg
NM_001282622.1:c.749T>G	NP_001269551.1:p.Met250Arg
NM_004187.3:c.752T>G	NP_004178.2:p.Met251Arg
XM_005262035.3:c.752T>G	XP_005262092.1:p.Met251Arg
XM_006724609.2:c.752T>G	XP_006724672.1:p.Met251Arg
XM_011530824.1:c.752T>G	XP_011529126.1:p.Met251Arg
XM_011530825.1:c.629T>G	XP_011529127.1:p.Met210Arg
XM_011530826.1:c.629T>G	XP_011529128.1:p.Met210Arg
XM_011530827.1:c.752T>G	XP_011529129.1:p.Met251Arg
XM_011530828.1:c.752T>G	XP_011529130.1:p.Met251Arg
XM_011530829.1:c.257T>G	XP_011529131.1:p.Met86Arg
XM_011530830.1:c.257T>G	XP_011529132.1:p.Met86Arg
XR_938369.1:n.1098T>G
XR_938370.1:n.1098T>G
XR_938371.1:n.1098T>G
XR_938372.1:n.1098T>G
XR_938373.1:n.1098T>G
NM_001353978.1:c.752T>G	NP_001340907.1:p.Met251Arg
NM_001353979.1:c.749T>G	NP_001340908.1:p.Met250Arg
NM_001353981.1:c.752T>G	NP_001340910.1:p.Met251Arg
NM_001353982.1:c.749T>G	NP_001340911.1:p.Met250Arg
NM_001353984.1:c.752T>G	NP_001340913.1:p.Met251Arg
NR_148672.1:n.1285T>G
NR_148673.1:n.1282T>G
NR_148674.1:n.1162T>G
XM_011530824.3:c.752T>G	XP_011529126.1:p.Met251Arg
XM_011530825.3:c.629T>G	XP_011529127.1:p.Met210Arg
XM_011530826.3:c.629T>G	XP_011529128.1:p.Met210Arg
XM_011530827.3:c.752T>G	XP_011529129.1:p.Met251Arg
XM_011530828.2:c.752T>G	XP_011529130.1:p.Met251Arg
XM_011530829.2:c.257T>G	XP_011529131.1:p.Met86Arg
XM_011530830.2:c.257T>G	XP_011529132.1:p.Met86Arg
XM_024452466.1:c.749T>G	XP_024308234.1:p.Met250Arg
XR_001755735.2:n.1078T>G
XR_001755736.2:n.1078T>G
XR_001755737.2:n.1078T>G
XR_938370.3:n.1078T>G
NM_001146702.2:c.551T>G	NP_001140174.1:p.Met184Arg
NM_001282622.3:c.749T>G	NP_001269551.1:p.Met250Arg
NM_001353978.3:c.752T>G	NP_001340907.1:p.Met251Arg
NM_001353979.2:c.749T>G	NP_001340908.1:p.Met250Arg
NM_001353981.2:c.752T>G	NP_001340910.1:p.Met251Arg
NM_001353982.2:c.749T>G	NP_001340911.1:p.Met250Arg
NM_004187.5:c.752T>G MANE Select	NP_004178.2:p.Met251Arg
NR_148672.2:n.1070T>G
NR_148673.2:n.1067T>G
NR_148674.2:n.947T>G
NM_001353984.2:c.752T>G	NP_001340913.1:p.Met251Arg