Canonical Allele Identifier: CA520160828

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21869856C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19707970C>A , CM000686.2:g.19707970C>A	GRCh38
NC_000024.9:g.21869856C>A , CM000686.1:g.21869856C>A	GRCh37
NC_000024.8:g.20329244C>A	NCBI36
NG_032920.1:g.41970G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000317961.9:c.3363G>T MANE Select	ENSP00000322408.4:p.Gly1121=
ENST00000317961.8:c.3363G>T	ENSP00000322408.4:p.Gly1121=
ENST00000382806.6:c.3192G>T	ENSP00000372256.2:p.Gly1064=
ENST00000415360.1:c.279G>T	ENSP00000389433.1:p.Gly93=
ENST00000440077.5:c.3240G>T	ENSP00000398543.1:p.Gly1080=
ENST00000469599.6:n.1961G>T
ENST00000492117.1:n.3255G>T
ENST00000541639.5:c.3456G>T	ENSP00000444293.1:p.Gly1152=
NM_001146705.1:c.3456G>T	NP_001140177.1:p.Gly1152=
NM_001146706.1:c.3192G>T	NP_001140178.1:p.Gly1064=
NM_004653.4:c.3363G>T	NP_004644.2:p.Gly1121=
XM_005262560.1:c.3228G>T	XP_005262617.1:p.Gly1076=
XM_005262561.1:c.3132G>T	XP_005262618.1:p.Gly1044=
XM_011531468.1:c.3285G>T	XP_011529770.1:p.Gly1095=
XR_244571.2:n.3651G>T
XR_430568.2:n.3985G>T
XM_005262560.3:c.3228G>T	XP_005262617.1:p.Gly1076=
XM_005262561.3:c.3132G>T	XP_005262618.1:p.Gly1044=
XM_011531468.3:c.3285G>T	XP_011529770.1:p.Gly1095=
XM_024452495.1:c.1353G>T	XP_024308263.1:p.Gly451=
XM_024452496.1:c.1119G>T	XP_024308264.1:p.Gly373=
XR_001756009.2:n.4101G>T
XR_001756010.2:n.4101G>T
XR_001756011.2:n.3966G>T
XR_001756012.2:n.4114G>T
XR_001756013.2:n.3432G>T
XR_002958832.1:n.3533G>T
XR_002958834.1:n.3757G>T
XR_002958835.1:n.3640G>T
XR_002958836.1:n.4323G>T
XR_002958837.1:n.4130G>T
XR_244571.4:n.3650G>T
XR_430568.4:n.3984G>T
NM_001146706.2:c.3192G>T	NP_001140178.1:p.Gly1064=
NM_004653.5:c.3363G>T MANE Select	NP_004644.2:p.Gly1121=
NM_001146705.2:c.3456G>T	NP_001140177.1:p.Gly1152=