Canonical Allele Identifier: CA520514703

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21868028A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19706142A>G , CM000686.2:g.19706142A>G	GRCh38
NC_000024.9:g.21868028A>G , CM000686.1:g.21868028A>G	GRCh37
NC_000024.8:g.20327416A>G	NCBI36
NG_032920.1:g.43798T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.4473T>C MANE Select	ENSP00000322408.4:p.Asn1491=
ENST00000317961.8:c.4473T>C	ENSP00000322408.4:p.Asn1491=
ENST00000382806.6:c.4302T>C	ENSP00000372256.2:p.Asn1434=
ENST00000440077.5:c.4350T>C	ENSP00000398543.1:p.Asn1450=
ENST00000469599.6:n.3224T>C
ENST00000492117.1:n.4518T>C
ENST00000541639.5:c.4566T>C	ENSP00000444293.1:p.Asn1522=
NM_001146705.1:c.4566T>C	NP_001140177.1:p.Asn1522=
NM_001146706.1:c.4302T>C	NP_001140178.1:p.Asn1434=
NM_004653.4:c.4473T>C	NP_004644.2:p.Asn1491=
XM_005262560.1:c.4338T>C	XP_005262617.1:p.Asn1446=
XM_005262561.1:c.4242T>C	XP_005262618.1:p.Asn1414=
XM_011531468.1:c.4395T>C	XP_011529770.1:p.Asn1465=
XR_430568.2:n.5248T>C
XM_005262560.3:c.4338T>C	XP_005262617.1:p.Asn1446=
XM_005262561.3:c.4242T>C	XP_005262618.1:p.Asn1414=
XM_011531468.3:c.4395T>C	XP_011529770.1:p.Asn1465=
XM_024452495.1:c.2463T>C	XP_024308263.1:p.Asn821=
XM_024452496.1:c.2229T>C	XP_024308264.1:p.Asn743=
XR_001756009.2:n.5211T>C
XR_001756010.2:n.5179T>C
XR_001756011.2:n.5076T>C
XR_001756012.2:n.5224T>C
XR_001756013.2:n.4542T>C
XR_002958832.1:n.4796T>C
XR_002958834.1:n.4867T>C
XR_002958835.1:n.4750T>C
XR_002958836.1:n.5401T>C
XR_002958837.1:n.5208T>C
XR_244571.4:n.4728T>C
XR_430568.4:n.5247T>C
NM_001146706.2:c.4302T>C	NP_001140178.1:p.Asn1434=
NM_004653.5:c.4473T>C MANE Select	NP_004644.2:p.Asn1491=
NM_001146705.2:c.4566T>C	NP_001140177.1:p.Asn1522=