Canonical Allele Identifier: CA367068483
Gene: HOXA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.27135054T>A (hg19) chr7:g.27095435T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27095435T>A , CM000669.2:g.27095435T>A GRCh38
NC_000007.13:g.27135054T>A , CM000669.1:g.27135054T>A GRCh37
NC_000007.12:g.27101579T>A NCBI36
NG_011813.1:g.5572A>T
NG_033087.1:g.4342T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000643460.2:c.478A>T MANE Select ENSP00000494260.2:p.Ile160Phe
ENST00000343060.4:c.478A>T ENSP00000343246.4:p.Ile160Phe
ENST00000355633.5:c.355-80A>T ENSP00000347851.5:n.355-80A>T
NM_005522.4:c.478A>T NP_005513.1:p.Ile160Phe
NM_153620.2:c.355-80A>T NP_705873.2:n.355-80A>T
NM_005522.5:c.478A>T MANE Select NP_005513.2:p.Ile160Phe
NM_153620.3:c.355-80A>T NP_705873.3:n.355-80A>T
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