Canonical Allele Identifier: CA520160881

Gene: KDM5D

Linked Data

• MyVariant Identifiers: chrY:g.21869940T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19708054T>C , CM000686.2:g.19708054T>C	GRCh38
NC_000024.9:g.21869940T>C , CM000686.1:g.21869940T>C	GRCh37
NC_000024.8:g.20329328T>C	NCBI36
NG_032920.1:g.41886A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317961.9:c.3279A>G MANE Select	ENSP00000322408.4:p.Ala1093=
ENST00000317961.8:c.3279A>G	ENSP00000322408.4:p.Ala1093=
ENST00000382806.6:c.3108A>G	ENSP00000372256.2:p.Ala1036=
ENST00000415360.1:c.195A>G	ENSP00000389433.1:p.Ala65=
ENST00000440077.5:c.3156A>G	ENSP00000398543.1:p.Ala1052=
ENST00000469599.6:n.1877A>G
ENST00000492117.1:n.3171A>G
ENST00000541639.5:c.3372A>G	ENSP00000444293.1:p.Ala1124=
NM_001146705.1:c.3372A>G	NP_001140177.1:p.Ala1124=
NM_001146706.1:c.3108A>G	NP_001140178.1:p.Ala1036=
NM_004653.4:c.3279A>G	NP_004644.2:p.Ala1093=
XM_005262560.1:c.3144A>G	XP_005262617.1:p.Ala1048=
XM_005262561.1:c.3048A>G	XP_005262618.1:p.Ala1016=
XM_011531468.1:c.3201A>G	XP_011529770.1:p.Ala1067=
XR_244571.2:n.3567A>G
XR_430568.2:n.3901A>G
XM_005262560.3:c.3144A>G	XP_005262617.1:p.Ala1048=
XM_005262561.3:c.3048A>G	XP_005262618.1:p.Ala1016=
XM_011531468.3:c.3201A>G	XP_011529770.1:p.Ala1067=
XM_024452495.1:c.1269A>G	XP_024308263.1:p.Ala423=
XM_024452496.1:c.1035A>G	XP_024308264.1:p.Ala345=
XR_001756009.2:n.4017A>G
XR_001756010.2:n.4017A>G
XR_001756011.2:n.3882A>G
XR_001756012.2:n.4030A>G
XR_001756013.2:n.3348A>G
XR_002958832.1:n.3449A>G
XR_002958834.1:n.3673A>G
XR_002958835.1:n.3556A>G
XR_002958836.1:n.4239A>G
XR_002958837.1:n.4046A>G
XR_244571.4:n.3566A>G
XR_430568.4:n.3900A>G
NM_001146706.2:c.3108A>G	NP_001140178.1:p.Ala1036=
NM_004653.5:c.3279A>G MANE Select	NP_004644.2:p.Ala1093=
NM_001146705.2:c.3372A>G	NP_001140177.1:p.Ala1124=