Canonical Allele Identifier: CA367069026

Gene: HOXA1

Linked Data

• MyVariant Identifiers: chr7:g.27135269A>C (hg19) ; chr7:g.27095650A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.27095650A>C , CM000669.2:g.27095650A>C	GRCh38
NC_000007.13:g.27135269A>C , CM000669.1:g.27135269A>C	GRCh37
NC_000007.12:g.27101794A>C	NCBI36
NG_011813.1:g.5357T>G
NG_033087.1:g.4557A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643460.2:c.263T>G MANE Select	ENSP00000494260.2:p.Val88Gly
ENST00000343060.4:c.263T>G	ENSP00000343246.4:p.Val88Gly
ENST00000355633.5:c.263T>G	ENSP00000347851.5:p.Val88Gly
NM_005522.4:c.263T>G	NP_005513.1:p.Val88Gly
NM_153620.2:c.263T>G	NP_705873.2:p.Val88Gly
NM_005522.5:c.263T>G MANE Select	NP_005513.2:p.Val88Gly
NM_153620.3:c.263T>G	NP_705873.3:p.Val88Gly