Canonical Allele Identifier: CA1696186897

Gene: HOXA1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.27095449C= , CM000669.2:g.27095449C=	GRCh38
NC_000007.13:g.27135068C= , CM000669.1:g.27135068C=	GRCh37
NC_000007.12:g.27101593C=	NCBI36
NG_011813.1:g.5558G=
NG_033087.1:g.4356C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000643460.2:c.464G= MANE Select	ENSP00000494260.2:p.Gly155=
ENST00000343060.4:c.464G=	ENSP00000343246.4:p.Gly155=
ENST00000355633.5:c.355-94G=	ENSP00000347851.5:n.355-94G=
NM_005522.4:c.464G=	NP_005513.1:p.Gly155=
NM_153620.2:c.355-94G=	NP_705873.2:n.355-94G=
NM_005522.5:c.464G= MANE Select	NP_005513.2:p.Gly155=
NM_153620.3:c.355-94G=	NP_705873.3:n.355-94G=