Canonical Allele Identifier: CA1696187539

Gene: HOXA1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.27095790C= , CM000669.2:g.27095790C=	GRCh38
NC_000007.13:g.27135409C= , CM000669.1:g.27135409C=	GRCh37
NC_000007.12:g.27101934C=	NCBI36
NG_011813.1:g.5217G=
NG_033087.1:g.4697C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643460.2:c.123G= MANE Select	ENSP00000494260.2:p.Ala41=
ENST00000343060.4:c.123G=	ENSP00000343246.4:p.Ala41=
ENST00000355633.5:c.123G=	ENSP00000347851.5:p.Ala41=
NM_005522.4:c.123G=	NP_005513.1:p.Ala41=
NM_153620.2:c.123G=	NP_705873.2:p.Ala41=
NM_005522.5:c.123G= MANE Select	NP_005513.2:p.Ala41=
NM_153620.3:c.123G=	NP_705873.3:p.Ala41=