Canonical Allele Identifier: CA520516664

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21869438C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19707552C>T , CM000686.2:g.19707552C>T	GRCh38
NC_000024.9:g.21869438C>T , CM000686.1:g.21869438C>T	GRCh37
NC_000024.8:g.20328826C>T	NCBI36
NG_032920.1:g.42388G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.3594G>A MANE Select	ENSP00000322408.4:p.Gly1198=
ENST00000317961.8:c.3594G>A	ENSP00000322408.4:p.Gly1198=
ENST00000382806.6:c.3423G>A	ENSP00000372256.2:p.Gly1141=
ENST00000415360.1:c.510G>A	ENSP00000389433.1:p.Gly170=
ENST00000440077.5:c.3471G>A	ENSP00000398543.1:p.Gly1157=
ENST00000469599.6:n.2192G>A
ENST00000492117.1:n.3486G>A
ENST00000541639.5:c.3687G>A	ENSP00000444293.1:p.Gly1229=
NM_001146705.1:c.3687G>A	NP_001140177.1:p.Gly1229=
NM_001146706.1:c.3423G>A	NP_001140178.1:p.Gly1141=
NM_004653.4:c.3594G>A	NP_004644.2:p.Gly1198=
XM_005262560.1:c.3459G>A	XP_005262617.1:p.Gly1153=
XM_005262561.1:c.3363G>A	XP_005262618.1:p.Gly1121=
XM_011531468.1:c.3516G>A	XP_011529770.1:p.Gly1172=
XR_244571.2:n.3882G>A
XR_430568.2:n.4216G>A
XM_005262560.3:c.3459G>A	XP_005262617.1:p.Gly1153=
XM_005262561.3:c.3363G>A	XP_005262618.1:p.Gly1121=
XM_011531468.3:c.3516G>A	XP_011529770.1:p.Gly1172=
XM_024452495.1:c.1584G>A	XP_024308263.1:p.Gly528=
XM_024452496.1:c.1350G>A	XP_024308264.1:p.Gly450=
XR_001756009.2:n.4332G>A
XR_001756010.2:n.4332G>A
XR_001756011.2:n.4197G>A
XR_001756012.2:n.4345G>A
XR_001756013.2:n.3663G>A
XR_002958832.1:n.3764G>A
XR_002958834.1:n.3988G>A
XR_002958835.1:n.3871G>A
XR_002958836.1:n.4554G>A
XR_002958837.1:n.4361G>A
XR_244571.4:n.3881G>A
XR_430568.4:n.4215G>A
NM_001146706.2:c.3423G>A	NP_001140178.1:p.Gly1141=
NM_004653.5:c.3594G>A MANE Select	NP_004644.2:p.Gly1198=
NM_001146705.2:c.3687G>A	NP_001140177.1:p.Gly1229=