Canonical Allele Identifier: CA367069419
Gene: HOXA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.27135375A>T (hg19) chr7:g.27095756A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27095756A>T , CM000669.2:g.27095756A>T GRCh38
NC_000007.13:g.27135375A>T , CM000669.1:g.27135375A>T GRCh37
NC_000007.12:g.27101900A>T NCBI36
NG_011813.1:g.5251T>A
NG_033087.1:g.4663A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000643460.2:c.157T>A MANE Select ENSP00000494260.2:p.Phe53Ile
ENST00000343060.4:c.157T>A ENSP00000343246.4:p.Phe53Ile
ENST00000355633.5:c.157T>A ENSP00000347851.5:p.Phe53Ile
NM_005522.4:c.157T>A NP_005513.1:p.Phe53Ile
NM_153620.2:c.157T>A NP_705873.2:p.Phe53Ile
NM_005522.5:c.157T>A MANE Select NP_005513.2:p.Phe53Ile
NM_153620.3:c.157T>A NP_705873.3:p.Phe53Ile
Search 100 bp 5'
Search 100 bp 3'