Canonical Allele Identifier: CA367068447
Gene: HOXA1 HGNC NCBI

Linked Data

COSMIC: COSM1726611
MyVariant Identifiers: chr7:g.27135038C>G (hg19) chr7:g.27095419C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27095419C>G , CM000669.2:g.27095419C>G GRCh38
NC_000007.13:g.27135038C>G , CM000669.1:g.27135038C>G GRCh37
NC_000007.12:g.27101563C>G NCBI36
NG_011813.1:g.5588G>C
NG_033087.1:g.4326C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000643460.2:c.494G>C MANE Select ENSP00000494260.2:p.Gly165Ala
ENST00000343060.4:c.494G>C ENSP00000343246.4:p.Gly165Ala
ENST00000355633.5:c.355-64G>C ENSP00000347851.5:n.355-64G>C
NM_005522.4:c.494G>C NP_005513.1:p.Gly165Ala
NM_153620.2:c.355-64G>C NP_705873.2:n.355-64G>C
NM_005522.5:c.494G>C MANE Select NP_005513.2:p.Gly165Ala
NM_153620.3:c.355-64G>C NP_705873.3:n.355-64G>C
Search 100 bp 5'
Search 100 bp 3'