Canonical Allele Identifier: CA1309431459

Gene: HOXD13

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.176093496C= , CM000664.2:g.176093496C=	GRCh38
NC_000002.11:g.176958224C= , CM000664.1:g.176958224C=	GRCh37
NC_000002.10:g.176666470C=	NCBI36
NG_008137.1:g.5693C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392539.4:c.606C= MANE Select	ENSP00000376322.3:p.His202=
ENST00000392539.3:c.606C=	ENSP00000376322.3:p.His202=
NM_000523.3:c.606C=	NP_000514.2:p.His202=
XM_011511068.1:c.725-984C=	XP_011509370.1:n.725-984C=
XM_011511068.2:c.725-984C=	XP_011509370.1:n.725-984C=
NM_000523.4:c.606C= MANE Select	NP_000514.2:p.His202=