Canonical Allele Identifier: CA520516929

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21869528G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19707642G>T , CM000686.2:g.19707642G>T	GRCh38
NC_000024.9:g.21869528G>T , CM000686.1:g.21869528G>T	GRCh37
NC_000024.8:g.20328916G>T	NCBI36
NG_032920.1:g.42298C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.3504C>A MANE Select	ENSP00000322408.4:p.Ala1168=
ENST00000317961.8:c.3504C>A	ENSP00000322408.4:p.Ala1168=
ENST00000382806.6:c.3333C>A	ENSP00000372256.2:p.Ala1111=
ENST00000415360.1:c.420C>A	ENSP00000389433.1:p.Ala140=
ENST00000440077.5:c.3381C>A	ENSP00000398543.1:p.Ala1127=
ENST00000469599.6:n.2102C>A
ENST00000492117.1:n.3396C>A
ENST00000541639.5:c.3597C>A	ENSP00000444293.1:p.Ala1199=
NM_001146705.1:c.3597C>A	NP_001140177.1:p.Ala1199=
NM_001146706.1:c.3333C>A	NP_001140178.1:p.Ala1111=
NM_004653.4:c.3504C>A	NP_004644.2:p.Ala1168=
XM_005262560.1:c.3369C>A	XP_005262617.1:p.Ala1123=
XM_005262561.1:c.3273C>A	XP_005262618.1:p.Ala1091=
XM_011531468.1:c.3426C>A	XP_011529770.1:p.Ala1142=
XR_244571.2:n.3792C>A
XR_430568.2:n.4126C>A
XM_005262560.3:c.3369C>A	XP_005262617.1:p.Ala1123=
XM_005262561.3:c.3273C>A	XP_005262618.1:p.Ala1091=
XM_011531468.3:c.3426C>A	XP_011529770.1:p.Ala1142=
XM_024452495.1:c.1494C>A	XP_024308263.1:p.Ala498=
XM_024452496.1:c.1260C>A	XP_024308264.1:p.Ala420=
XR_001756009.2:n.4242C>A
XR_001756010.2:n.4242C>A
XR_001756011.2:n.4107C>A
XR_001756012.2:n.4255C>A
XR_001756013.2:n.3573C>A
XR_002958832.1:n.3674C>A
XR_002958834.1:n.3898C>A
XR_002958835.1:n.3781C>A
XR_002958836.1:n.4464C>A
XR_002958837.1:n.4271C>A
XR_244571.4:n.3791C>A
XR_430568.4:n.4125C>A
NM_001146706.2:c.3333C>A	NP_001140178.1:p.Ala1111=
NM_004653.5:c.3504C>A MANE Select	NP_004644.2:p.Ala1168=
NM_001146705.2:c.3597C>A	NP_001140177.1:p.Ala1199=