Canonical Allele Identifier: CA367069021
Gene: HOXA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.27135267A>T (hg19) chr7:g.27095648A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27095648A>T , CM000669.2:g.27095648A>T GRCh38
NC_000007.13:g.27135267A>T , CM000669.1:g.27135267A>T GRCh37
NC_000007.12:g.27101792A>T NCBI36
NG_011813.1:g.5359T>A
NG_033087.1:g.4555A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000643460.2:c.265T>A MANE Select ENSP00000494260.2:p.Ser89Thr
ENST00000343060.4:c.265T>A ENSP00000343246.4:p.Ser89Thr
ENST00000355633.5:c.265T>A ENSP00000347851.5:p.Ser89Thr
NM_005522.4:c.265T>A NP_005513.1:p.Ser89Thr
NM_153620.2:c.265T>A NP_705873.2:p.Ser89Thr
NM_005522.5:c.265T>A MANE Select NP_005513.2:p.Ser89Thr
NM_153620.3:c.265T>A NP_705873.3:p.Ser89Thr
Search 100 bp 5'
Search 100 bp 3'