Canonical Allele Identifier: CA520160788

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21869618C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19707732C>T , CM000686.2:g.19707732C>T	GRCh38
NC_000024.9:g.21869618C>T , CM000686.1:g.21869618C>T	GRCh37
NC_000024.8:g.20329006C>T	NCBI36
NG_032920.1:g.42208G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.3414G>A MANE Select	ENSP00000322408.4:p.Lys1138=
ENST00000317961.8:c.3414G>A	ENSP00000322408.4:p.Lys1138=
ENST00000382806.6:c.3243G>A	ENSP00000372256.2:p.Lys1081=
ENST00000415360.1:c.330G>A	ENSP00000389433.1:p.Lys110=
ENST00000440077.5:c.3291G>A	ENSP00000398543.1:p.Lys1097=
ENST00000469599.6:n.2012G>A
ENST00000492117.1:n.3306G>A
ENST00000541639.5:c.3507G>A	ENSP00000444293.1:p.Lys1169=
NM_001146705.1:c.3507G>A	NP_001140177.1:p.Lys1169=
NM_001146706.1:c.3243G>A	NP_001140178.1:p.Lys1081=
NM_004653.4:c.3414G>A	NP_004644.2:p.Lys1138=
XM_005262560.1:c.3279G>A	XP_005262617.1:p.Lys1093=
XM_005262561.1:c.3183G>A	XP_005262618.1:p.Lys1061=
XM_011531468.1:c.3336G>A	XP_011529770.1:p.Lys1112=
XR_244571.2:n.3702G>A
XR_430568.2:n.4036G>A
XM_005262560.3:c.3279G>A	XP_005262617.1:p.Lys1093=
XM_005262561.3:c.3183G>A	XP_005262618.1:p.Lys1061=
XM_011531468.3:c.3336G>A	XP_011529770.1:p.Lys1112=
XM_024452495.1:c.1404G>A	XP_024308263.1:p.Lys468=
XM_024452496.1:c.1170G>A	XP_024308264.1:p.Lys390=
XR_001756009.2:n.4152G>A
XR_001756010.2:n.4152G>A
XR_001756011.2:n.4017G>A
XR_001756012.2:n.4165G>A
XR_001756013.2:n.3483G>A
XR_002958832.1:n.3584G>A
XR_002958834.1:n.3808G>A
XR_002958835.1:n.3691G>A
XR_002958836.1:n.4374G>A
XR_002958837.1:n.4181G>A
XR_244571.4:n.3701G>A
XR_430568.4:n.4035G>A
NM_001146706.2:c.3243G>A	NP_001140178.1:p.Lys1081=
NM_004653.5:c.3414G>A MANE Select	NP_004644.2:p.Lys1138=
NM_001146705.2:c.3507G>A	NP_001140177.1:p.Lys1169=