Canonical Allele Identifier: CA367068482
Gene: HOXA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.27135053A>T (hg19) chr7:g.27095434A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27095434A>T , CM000669.2:g.27095434A>T GRCh38
NC_000007.13:g.27135053A>T , CM000669.1:g.27135053A>T GRCh37
NC_000007.12:g.27101578A>T NCBI36
NG_011813.1:g.5573T>A
NG_033087.1:g.4341A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000643460.2:c.479T>A MANE Select ENSP00000494260.2:p.Ile160Asn
ENST00000343060.4:c.479T>A ENSP00000343246.4:p.Ile160Asn
ENST00000355633.5:c.355-79T>A ENSP00000347851.5:n.355-79T>A
NM_005522.4:c.479T>A NP_005513.1:p.Ile160Asn
NM_153620.2:c.355-79T>A NP_705873.2:n.355-79T>A
NM_005522.5:c.479T>A MANE Select NP_005513.2:p.Ile160Asn
NM_153620.3:c.355-79T>A NP_705873.3:n.355-79T>A
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