Canonical Allele Identifier: CA520516452

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21869324G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19707438G>T , CM000686.2:g.19707438G>T	GRCh38
NC_000024.9:g.21869324G>T , CM000686.1:g.21869324G>T	GRCh37
NC_000024.8:g.20328712G>T	NCBI36
NG_032920.1:g.42502C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.3708C>A MANE Select	ENSP00000322408.4:p.Arg1236=
ENST00000317961.8:c.3708C>A	ENSP00000322408.4:p.Arg1236=
ENST00000382806.6:c.3537C>A	ENSP00000372256.2:p.Arg1179=
ENST00000415360.1:c.624C>A	ENSP00000389433.1:p.Arg208=
ENST00000440077.5:c.3585C>A	ENSP00000398543.1:p.Arg1195=
ENST00000469599.6:n.2306C>A
ENST00000492117.1:n.3600C>A
ENST00000541639.5:c.3801C>A	ENSP00000444293.1:p.Arg1267=
NM_001146705.1:c.3801C>A	NP_001140177.1:p.Arg1267=
NM_001146706.1:c.3537C>A	NP_001140178.1:p.Arg1179=
NM_004653.4:c.3708C>A	NP_004644.2:p.Arg1236=
XM_005262560.1:c.3573C>A	XP_005262617.1:p.Arg1191=
XM_005262561.1:c.3477C>A	XP_005262618.1:p.Arg1159=
XM_011531468.1:c.3630C>A	XP_011529770.1:p.Arg1210=
XR_244571.2:n.3996C>A
XR_430568.2:n.4330C>A
XM_005262560.3:c.3573C>A	XP_005262617.1:p.Arg1191=
XM_005262561.3:c.3477C>A	XP_005262618.1:p.Arg1159=
XM_011531468.3:c.3630C>A	XP_011529770.1:p.Arg1210=
XM_024452495.1:c.1698C>A	XP_024308263.1:p.Arg566=
XM_024452496.1:c.1464C>A	XP_024308264.1:p.Arg488=
XR_001756009.2:n.4446C>A
XR_001756010.2:n.4446C>A
XR_001756011.2:n.4311C>A
XR_001756012.2:n.4459C>A
XR_001756013.2:n.3777C>A
XR_002958832.1:n.3878C>A
XR_002958834.1:n.4102C>A
XR_002958835.1:n.3985C>A
XR_002958836.1:n.4668C>A
XR_002958837.1:n.4475C>A
XR_244571.4:n.3995C>A
XR_430568.4:n.4329C>A
NM_001146706.2:c.3537C>A	NP_001140178.1:p.Arg1179=
NM_004653.5:c.3708C>A MANE Select	NP_004644.2:p.Arg1236=
NM_001146705.2:c.3801C>A	NP_001140177.1:p.Arg1267=