Canonical Allele Identifier: CA520516785

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21869477T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19707591T>A , CM000686.2:g.19707591T>A	GRCh38
NC_000024.9:g.21869477T>A , CM000686.1:g.21869477T>A	GRCh37
NC_000024.8:g.20328865T>A	NCBI36
NG_032920.1:g.42349A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.3555A>T MANE Select	ENSP00000322408.4:p.Gly1185=
ENST00000317961.8:c.3555A>T	ENSP00000322408.4:p.Gly1185=
ENST00000382806.6:c.3384A>T	ENSP00000372256.2:p.Gly1128=
ENST00000415360.1:c.471A>T	ENSP00000389433.1:p.Gly157=
ENST00000440077.5:c.3432A>T	ENSP00000398543.1:p.Gly1144=
ENST00000469599.6:n.2153A>T
ENST00000492117.1:n.3447A>T
ENST00000541639.5:c.3648A>T	ENSP00000444293.1:p.Gly1216=
NM_001146705.1:c.3648A>T	NP_001140177.1:p.Gly1216=
NM_001146706.1:c.3384A>T	NP_001140178.1:p.Gly1128=
NM_004653.4:c.3555A>T	NP_004644.2:p.Gly1185=
XM_005262560.1:c.3420A>T	XP_005262617.1:p.Gly1140=
XM_005262561.1:c.3324A>T	XP_005262618.1:p.Gly1108=
XM_011531468.1:c.3477A>T	XP_011529770.1:p.Gly1159=
XR_244571.2:n.3843A>T
XR_430568.2:n.4177A>T
XM_005262560.3:c.3420A>T	XP_005262617.1:p.Gly1140=
XM_005262561.3:c.3324A>T	XP_005262618.1:p.Gly1108=
XM_011531468.3:c.3477A>T	XP_011529770.1:p.Gly1159=
XM_024452495.1:c.1545A>T	XP_024308263.1:p.Gly515=
XM_024452496.1:c.1311A>T	XP_024308264.1:p.Gly437=
XR_001756009.2:n.4293A>T
XR_001756010.2:n.4293A>T
XR_001756011.2:n.4158A>T
XR_001756012.2:n.4306A>T
XR_001756013.2:n.3624A>T
XR_002958832.1:n.3725A>T
XR_002958834.1:n.3949A>T
XR_002958835.1:n.3832A>T
XR_002958836.1:n.4515A>T
XR_002958837.1:n.4322A>T
XR_244571.4:n.3842A>T
XR_430568.4:n.4176A>T
NM_001146706.2:c.3384A>T	NP_001140178.1:p.Gly1128=
NM_004653.5:c.3555A>T MANE Select	NP_004644.2:p.Gly1185=
NM_001146705.2:c.3648A>T	NP_001140177.1:p.Gly1216=