Canonical Allele Identifier: CA520516813

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21869486A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19707600A>C , CM000686.2:g.19707600A>C	GRCh38
NC_000024.9:g.21869486A>C , CM000686.1:g.21869486A>C	GRCh37
NC_000024.8:g.20328874A>C	NCBI36
NG_032920.1:g.42340T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.3546T>G MANE Select	ENSP00000322408.4:p.Ala1182=
ENST00000317961.8:c.3546T>G	ENSP00000322408.4:p.Ala1182=
ENST00000382806.6:c.3375T>G	ENSP00000372256.2:p.Ala1125=
ENST00000415360.1:c.462T>G	ENSP00000389433.1:p.Ala154=
ENST00000440077.5:c.3423T>G	ENSP00000398543.1:p.Ala1141=
ENST00000469599.6:n.2144T>G
ENST00000492117.1:n.3438T>G
ENST00000541639.5:c.3639T>G	ENSP00000444293.1:p.Ala1213=
NM_001146705.1:c.3639T>G	NP_001140177.1:p.Ala1213=
NM_001146706.1:c.3375T>G	NP_001140178.1:p.Ala1125=
NM_004653.4:c.3546T>G	NP_004644.2:p.Ala1182=
XM_005262560.1:c.3411T>G	XP_005262617.1:p.Ala1137=
XM_005262561.1:c.3315T>G	XP_005262618.1:p.Ala1105=
XM_011531468.1:c.3468T>G	XP_011529770.1:p.Ala1156=
XR_244571.2:n.3834T>G
XR_430568.2:n.4168T>G
XM_005262560.3:c.3411T>G	XP_005262617.1:p.Ala1137=
XM_005262561.3:c.3315T>G	XP_005262618.1:p.Ala1105=
XM_011531468.3:c.3468T>G	XP_011529770.1:p.Ala1156=
XM_024452495.1:c.1536T>G	XP_024308263.1:p.Ala512=
XM_024452496.1:c.1302T>G	XP_024308264.1:p.Ala434=
XR_001756009.2:n.4284T>G
XR_001756010.2:n.4284T>G
XR_001756011.2:n.4149T>G
XR_001756012.2:n.4297T>G
XR_001756013.2:n.3615T>G
XR_002958832.1:n.3716T>G
XR_002958834.1:n.3940T>G
XR_002958835.1:n.3823T>G
XR_002958836.1:n.4506T>G
XR_002958837.1:n.4313T>G
XR_244571.4:n.3833T>G
XR_430568.4:n.4167T>G
NM_001146706.2:c.3375T>G	NP_001140178.1:p.Ala1125=
NM_004653.5:c.3546T>G MANE Select	NP_004644.2:p.Ala1182=
NM_001146705.2:c.3639T>G	NP_001140177.1:p.Ala1213=