Canonical Allele Identifier: CA2470921471

Gene: KDM5D

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19744281_19744282delinsAG , CM000686.2:g.19744281_19744282delinsAG	GRCh38
NC_000024.9:g.21906167_21906168delinsAG , CM000686.1:g.21906167_21906168delinsAG	GRCh37
NC_000024.8:g.20365555_20365556delinsAG	NCBI36
NG_032920.1:g.5658_5659delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000317961.9:c.150+103_150+104delinsCT MANE Select	ENSP00000322408.4:n.150+103_150+104delins...
ENST00000317961.8:c.150+103_150+104delinsCT	ENSP00000322408.4:n.150+103_150+104delins...
ENST00000382806.6:c.150+103_150+104delinsCT	ENSP00000372256.2:n.150+103_150+104delins...
ENST00000440077.5:c.150+103_150+104delinsCT	ENSP00000398543.1:n.150+103_150+104delins...
ENST00000447300.1:c.150+103_150+104delinsCT	ENSP00000416377.1:n.150+103_150+104delins...
ENST00000541639.5:c.150+103_150+104delinsCT	ENSP00000444293.1:n.150+103_150+104delins...
NM_001146705.1:c.150+103_150+104delinsCT	NP_001140177.1:n.150+103_150+104delinsCT
NM_001146706.1:c.150+103_150+104delinsCT	NP_001140178.1:n.150+103_150+104delinsCT
NM_004653.4:c.150+103_150+104delinsCT	NP_004644.2:n.150+103_150+104delinsCT
XM_005262560.1:c.150+103_150+104delinsCT	XP_005262617.1:n.150+103_150+104delinsCT
XM_005262561.1:c.150+103_150+104delinsCT	XP_005262618.1:n.150+103_150+104delinsCT
XM_005262562.2:c.150+103_150+104delinsCT	XP_005262619.1:n.150+103_150+104delinsCT
XM_011531468.1:c.150+103_150+104delinsCT	XP_011529770.1:n.150+103_150+104delinsCT
XR_244571.2:n.438+103_438+104delinsCT
XR_430568.2:n.438+103_438+104delinsCT
XR_938609.1:n.438+103_438+104delinsCT
XR_938610.1:n.438+103_438+104delinsCT
XM_005262560.3:c.150+103_150+104delinsCT	XP_005262617.1:n.150+103_150+104delinsCT
XM_005262561.3:c.150+103_150+104delinsCT	XP_005262618.1:n.150+103_150+104delinsCT
XM_011531468.3:c.150+103_150+104delinsCT	XP_011529770.1:n.150+103_150+104delinsCT
XM_024452495.1:c.-1833+103_-1833+104delinsCT	XP_024308263.1:n.-1833+103_-1833+104delin...
XR_001756009.2:n.437+103_437+104delinsCT
XR_001756010.2:n.437+103_437+104delinsCT
XR_001756011.2:n.437+103_437+104delinsCT
XR_001756012.2:n.437+103_437+104delinsCT
XR_001756013.2:n.437+103_437+104delinsCT
XR_002958832.1:n.437+103_437+104delinsCT
XR_002958833.1:n.437+103_437+104delinsCT
XR_002958834.1:n.437+103_437+104delinsCT
XR_002958835.1:n.437+103_437+104delinsCT
XR_002958836.1:n.437+103_437+104delinsCT
XR_002958837.1:n.437+103_437+104delinsCT
XR_244571.4:n.437+103_437+104delinsCT
XR_430568.4:n.437+103_437+104delinsCT
NM_001146706.2:c.150+103_150+104delinsCT	NP_001140178.1:n.150+103_150+104delinsCT
NM_004653.5:c.150+103_150+104delinsCT MANE Select	NP_004644.2:n.150+103_150+104delinsCT
NM_001146705.2:c.150+103_150+104delinsCT	NP_001140177.1:n.150+103_150+104delinsCT