Canonical Allele Identifier: CA520160766

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21869579C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19707693C>T , CM000686.2:g.19707693C>T	GRCh38
NC_000024.9:g.21869579C>T , CM000686.1:g.21869579C>T	GRCh37
NC_000024.8:g.20328967C>T	NCBI36
NG_032920.1:g.42247G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.3453G>A MANE Select	ENSP00000322408.4:p.Leu1151=
ENST00000317961.8:c.3453G>A	ENSP00000322408.4:p.Leu1151=
ENST00000382806.6:c.3282G>A	ENSP00000372256.2:p.Leu1094=
ENST00000415360.1:c.369G>A	ENSP00000389433.1:p.Leu123=
ENST00000440077.5:c.3330G>A	ENSP00000398543.1:p.Leu1110=
ENST00000469599.6:n.2051G>A
ENST00000492117.1:n.3345G>A
ENST00000541639.5:c.3546G>A	ENSP00000444293.1:p.Leu1182=
NM_001146705.1:c.3546G>A	NP_001140177.1:p.Leu1182=
NM_001146706.1:c.3282G>A	NP_001140178.1:p.Leu1094=
NM_004653.4:c.3453G>A	NP_004644.2:p.Leu1151=
XM_005262560.1:c.3318G>A	XP_005262617.1:p.Leu1106=
XM_005262561.1:c.3222G>A	XP_005262618.1:p.Leu1074=
XM_011531468.1:c.3375G>A	XP_011529770.1:p.Leu1125=
XR_244571.2:n.3741G>A
XR_430568.2:n.4075G>A
XM_005262560.3:c.3318G>A	XP_005262617.1:p.Leu1106=
XM_005262561.3:c.3222G>A	XP_005262618.1:p.Leu1074=
XM_011531468.3:c.3375G>A	XP_011529770.1:p.Leu1125=
XM_024452495.1:c.1443G>A	XP_024308263.1:p.Leu481=
XM_024452496.1:c.1209G>A	XP_024308264.1:p.Leu403=
XR_001756009.2:n.4191G>A
XR_001756010.2:n.4191G>A
XR_001756011.2:n.4056G>A
XR_001756012.2:n.4204G>A
XR_001756013.2:n.3522G>A
XR_002958832.1:n.3623G>A
XR_002958834.1:n.3847G>A
XR_002958835.1:n.3730G>A
XR_002958836.1:n.4413G>A
XR_002958837.1:n.4220G>A
XR_244571.4:n.3740G>A
XR_430568.4:n.4074G>A
NM_001146706.2:c.3282G>A	NP_001140178.1:p.Leu1094=
NM_004653.5:c.3453G>A MANE Select	NP_004644.2:p.Leu1151=
NM_001146705.2:c.3546G>A	NP_001140177.1:p.Leu1182=