Canonical Allele Identifier: CA520160020

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21868714G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19706828G>A , CM000686.2:g.19706828G>A	GRCh38
NC_000024.9:g.21868714G>A , CM000686.1:g.21868714G>A	GRCh37
NC_000024.8:g.20328102G>A	NCBI36
NG_032920.1:g.43112C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.4035C>T MANE Select	ENSP00000322408.4:p.Thr1345=
ENST00000317961.8:c.4035C>T	ENSP00000322408.4:p.Thr1345=
ENST00000382806.6:c.3864C>T	ENSP00000372256.2:p.Thr1288=
ENST00000440077.5:c.3912C>T	ENSP00000398543.1:p.Thr1304=
ENST00000469599.6:n.2633C>T
ENST00000492117.1:n.3927C>T
ENST00000541639.5:c.4128C>T	ENSP00000444293.1:p.Thr1376=
NM_001146705.1:c.4128C>T	NP_001140177.1:p.Thr1376=
NM_001146706.1:c.3864C>T	NP_001140178.1:p.Thr1288=
NM_004653.4:c.4035C>T	NP_004644.2:p.Thr1345=
XM_005262560.1:c.3900C>T	XP_005262617.1:p.Thr1300=
XM_005262561.1:c.3804C>T	XP_005262618.1:p.Thr1268=
XM_011531468.1:c.3957C>T	XP_011529770.1:p.Thr1319=
XR_244571.2:n.4323C>T
XR_430568.2:n.4657C>T
XM_005262560.3:c.3900C>T	XP_005262617.1:p.Thr1300=
XM_005262561.3:c.3804C>T	XP_005262618.1:p.Thr1268=
XM_011531468.3:c.3957C>T	XP_011529770.1:p.Thr1319=
XM_024452495.1:c.2025C>T	XP_024308263.1:p.Thr675=
XM_024452496.1:c.1791C>T	XP_024308264.1:p.Thr597=
XR_001756009.2:n.4773C>T
XR_001756010.2:n.4773C>T
XR_001756011.2:n.4638C>T
XR_001756012.2:n.4786C>T
XR_001756013.2:n.4104C>T
XR_002958832.1:n.4205C>T
XR_002958834.1:n.4429C>T
XR_002958835.1:n.4312C>T
XR_002958836.1:n.4995C>T
XR_002958837.1:n.4802C>T
XR_244571.4:n.4322C>T
XR_430568.4:n.4656C>T
NM_001146706.2:c.3864C>T	NP_001140178.1:p.Thr1288=
NM_004653.5:c.4035C>T MANE Select	NP_004644.2:p.Thr1345=
NM_001146705.2:c.4128C>T	NP_001140177.1:p.Thr1376=