Canonical Allele Identifier: CA520516740

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21869459C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19707573C>T , CM000686.2:g.19707573C>T	GRCh38
NC_000024.9:g.21869459C>T , CM000686.1:g.21869459C>T	GRCh37
NC_000024.8:g.20328847C>T	NCBI36
NG_032920.1:g.42367G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.3573G>A MANE Select	ENSP00000322408.4:p.Leu1191=
ENST00000317961.8:c.3573G>A	ENSP00000322408.4:p.Leu1191=
ENST00000382806.6:c.3402G>A	ENSP00000372256.2:p.Leu1134=
ENST00000415360.1:c.489G>A	ENSP00000389433.1:p.Leu163=
ENST00000440077.5:c.3450G>A	ENSP00000398543.1:p.Leu1150=
ENST00000469599.6:n.2171G>A
ENST00000492117.1:n.3465G>A
ENST00000541639.5:c.3666G>A	ENSP00000444293.1:p.Leu1222=
NM_001146705.1:c.3666G>A	NP_001140177.1:p.Leu1222=
NM_001146706.1:c.3402G>A	NP_001140178.1:p.Leu1134=
NM_004653.4:c.3573G>A	NP_004644.2:p.Leu1191=
XM_005262560.1:c.3438G>A	XP_005262617.1:p.Leu1146=
XM_005262561.1:c.3342G>A	XP_005262618.1:p.Leu1114=
XM_011531468.1:c.3495G>A	XP_011529770.1:p.Leu1165=
XR_244571.2:n.3861G>A
XR_430568.2:n.4195G>A
XM_005262560.3:c.3438G>A	XP_005262617.1:p.Leu1146=
XM_005262561.3:c.3342G>A	XP_005262618.1:p.Leu1114=
XM_011531468.3:c.3495G>A	XP_011529770.1:p.Leu1165=
XM_024452495.1:c.1563G>A	XP_024308263.1:p.Leu521=
XM_024452496.1:c.1329G>A	XP_024308264.1:p.Leu443=
XR_001756009.2:n.4311G>A
XR_001756010.2:n.4311G>A
XR_001756011.2:n.4176G>A
XR_001756012.2:n.4324G>A
XR_001756013.2:n.3642G>A
XR_002958832.1:n.3743G>A
XR_002958834.1:n.3967G>A
XR_002958835.1:n.3850G>A
XR_002958836.1:n.4533G>A
XR_002958837.1:n.4340G>A
XR_244571.4:n.3860G>A
XR_430568.4:n.4194G>A
NM_001146706.2:c.3402G>A	NP_001140178.1:p.Leu1134=
NM_004653.5:c.3573G>A MANE Select	NP_004644.2:p.Leu1191=
NM_001146705.2:c.3666G>A	NP_001140177.1:p.Leu1222=