Canonical Allele Identifier: CA454507638

Gene: HOXA1

Linked Data

• COSMIC: COSM118379
• MyVariant Identifiers: chr7:g.27135280C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.27095661C>A , CM000669.2:g.27095661C>A	GRCh38
NC_000007.13:g.27135280C>A , CM000669.1:g.27135280C>A	GRCh37
NC_000007.12:g.27101805C>A	NCBI36
NG_011813.1:g.5346G>T
NG_033087.1:g.4568C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643460.2:c.252G>T MANE Select	ENSP00000494260.2:p.Gly84=
ENST00000343060.4:c.252G>T	ENSP00000343246.4:p.Gly84=
ENST00000355633.5:c.252G>T	ENSP00000347851.5:p.Gly84=
NM_005522.4:c.252G>T	NP_005513.1:p.Gly84=
NM_153620.2:c.252G>T	NP_705873.2:p.Gly84=
NM_005522.5:c.252G>T MANE Select	NP_005513.2:p.Gly84=
NM_153620.3:c.252G>T	NP_705873.3:p.Gly84=