Canonical Allele Identifier: CA454507619

Gene: HOXA1

Linked Data

• MyVariant Identifiers: chr7:g.27135253T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.27095634T>A , CM000669.2:g.27095634T>A	GRCh38
NC_000007.13:g.27135253T>A , CM000669.1:g.27135253T>A	GRCh37
NC_000007.12:g.27101778T>A	NCBI36
NG_011813.1:g.5373A>T
NG_033087.1:g.4541T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000643460.2:c.279A>T MANE Select	ENSP00000494260.2:p.Ser93=
ENST00000343060.4:c.279A>T	ENSP00000343246.4:p.Ser93=
ENST00000355633.5:c.279A>T	ENSP00000347851.5:p.Ser93=
NM_005522.4:c.279A>T	NP_005513.1:p.Ser93=
NM_153620.2:c.279A>T	NP_705873.2:p.Ser93=
NM_005522.5:c.279A>T MANE Select	NP_005513.2:p.Ser93=
NM_153620.3:c.279A>T	NP_705873.3:p.Ser93=