Canonical Allele Identifier: CA520159346

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21867950G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19706064G>A , CM000686.2:g.19706064G>A	GRCh38
NC_000024.9:g.21867950G>A , CM000686.1:g.21867950G>A	GRCh37
NC_000024.8:g.20327338G>A	NCBI36
NG_032920.1:g.43876C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.4551C>T MANE Select	ENSP00000322408.4:p.Gly1517=
ENST00000317961.8:c.4551C>T	ENSP00000322408.4:p.Gly1517=
ENST00000382806.6:c.4380C>T	ENSP00000372256.2:p.Gly1460=
ENST00000440077.5:c.4428C>T	ENSP00000398543.1:p.Gly1476=
ENST00000469599.6:n.3302C>T
ENST00000492117.1:n.4596C>T
ENST00000541639.5:c.4644C>T	ENSP00000444293.1:p.Gly1548=
NM_001146705.1:c.4644C>T	NP_001140177.1:p.Gly1548=
NM_001146706.1:c.4380C>T	NP_001140178.1:p.Gly1460=
NM_004653.4:c.4551C>T	NP_004644.2:p.Gly1517=
XM_005262560.1:c.4416C>T	XP_005262617.1:p.Gly1472=
XM_005262561.1:c.4320C>T	XP_005262618.1:p.Gly1440=
XM_011531468.1:c.4473C>T	XP_011529770.1:p.Gly1491=
XR_430568.2:n.5326C>T
XM_005262560.3:c.4416C>T	XP_005262617.1:p.Gly1472=
XM_005262561.3:c.4320C>T	XP_005262618.1:p.Gly1440=
XM_011531468.3:c.4473C>T	XP_011529770.1:p.Gly1491=
XM_024452495.1:c.2541C>T	XP_024308263.1:p.Gly847=
XM_024452496.1:c.2307C>T	XP_024308264.1:p.Gly769=
XR_001756009.2:n.5289C>T
XR_001756010.2:n.5257C>T
XR_001756011.2:n.5154C>T
XR_001756012.2:n.5302C>T
XR_001756013.2:n.4620C>T
XR_002958832.1:n.4874C>T
XR_002958834.1:n.4945C>T
XR_002958835.1:n.4828C>T
XR_002958836.1:n.5479C>T
XR_002958837.1:n.5286C>T
XR_244571.4:n.4806C>T
XR_430568.4:n.5325C>T
NM_001146706.2:c.4380C>T	NP_001140178.1:p.Gly1460=
NM_004653.5:c.4551C>T MANE Select	NP_004644.2:p.Gly1517=
NM_001146705.2:c.4644C>T	NP_001140177.1:p.Gly1548=