Canonical Allele Identifier: CA367068557

Gene: HOXA1

Linked Data

• dbSNP Id: rs1488088492
• MyVariant Identifiers: chr7:g.27135089C>A (hg19) ; chr7:g.27095470C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.27095470C>A , CM000669.2:g.27095470C>A	GRCh38
NC_000007.13:g.27135089C>A , CM000669.1:g.27135089C>A	GRCh37
NC_000007.12:g.27101614C>A	NCBI36
NG_011813.1:g.5537G>T
NG_033087.1:g.4377C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643460.2:c.443G>T MANE Select	ENSP00000494260.2:p.Gly148Val
ENST00000343060.4:c.443G>T	ENSP00000343246.4:p.Gly148Val
ENST00000355633.5:c.354+89G>T	ENSP00000347851.5:n.354+89G>T
NM_005522.4:c.443G>T	NP_005513.1:p.Gly148Val
NM_153620.2:c.354+89G>T	NP_705873.2:n.354+89G>T
NM_005522.5:c.443G>T MANE Select	NP_005513.2:p.Gly148Val
NM_153620.3:c.354+89G>T	NP_705873.3:n.354+89G>T