Canonical Allele Identifier: CA520516442

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21869317G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19707431G>T , CM000686.2:g.19707431G>T	GRCh38
NC_000024.9:g.21869317G>T , CM000686.1:g.21869317G>T	GRCh37
NC_000024.8:g.20328705G>T	NCBI36
NG_032920.1:g.42509C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.3715C>A MANE Select	ENSP00000322408.4:p.Arg1239=
ENST00000317961.8:c.3715C>A	ENSP00000322408.4:p.Arg1239=
ENST00000382806.6:c.3544C>A	ENSP00000372256.2:p.Arg1182=
ENST00000415360.1:c.631C>A	ENSP00000389433.1:p.Arg211=
ENST00000440077.5:c.3592C>A	ENSP00000398543.1:p.Arg1198=
ENST00000469599.6:n.2313C>A
ENST00000492117.1:n.3607C>A
ENST00000541639.5:c.3808C>A	ENSP00000444293.1:p.Arg1270=
NM_001146705.1:c.3808C>A	NP_001140177.1:p.Arg1270=
NM_001146706.1:c.3544C>A	NP_001140178.1:p.Arg1182=
NM_004653.4:c.3715C>A	NP_004644.2:p.Arg1239=
XM_005262560.1:c.3580C>A	XP_005262617.1:p.Arg1194=
XM_005262561.1:c.3484C>A	XP_005262618.1:p.Arg1162=
XM_011531468.1:c.3637C>A	XP_011529770.1:p.Arg1213=
XR_244571.2:n.4003C>A
XR_430568.2:n.4337C>A
XM_005262560.3:c.3580C>A	XP_005262617.1:p.Arg1194=
XM_005262561.3:c.3484C>A	XP_005262618.1:p.Arg1162=
XM_011531468.3:c.3637C>A	XP_011529770.1:p.Arg1213=
XM_024452495.1:c.1705C>A	XP_024308263.1:p.Arg569=
XM_024452496.1:c.1471C>A	XP_024308264.1:p.Arg491=
XR_001756009.2:n.4453C>A
XR_001756010.2:n.4453C>A
XR_001756011.2:n.4318C>A
XR_001756012.2:n.4466C>A
XR_001756013.2:n.3784C>A
XR_002958832.1:n.3885C>A
XR_002958834.1:n.4109C>A
XR_002958835.1:n.3992C>A
XR_002958836.1:n.4675C>A
XR_002958837.1:n.4482C>A
XR_244571.4:n.4002C>A
XR_430568.4:n.4336C>A
NM_001146706.2:c.3544C>A	NP_001140178.1:p.Arg1182=
NM_004653.5:c.3715C>A MANE Select	NP_004644.2:p.Arg1239=
NM_001146705.2:c.3808C>A	NP_001140177.1:p.Arg1270=