Canonical Allele Identifier: CA454507649
Gene: HOXA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.27135040A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27095421A>G , CM000669.2:g.27095421A>G GRCh38
NC_000007.13:g.27135040A>G , CM000669.1:g.27135040A>G GRCh37
NC_000007.12:g.27101565A>G NCBI36
NG_011813.1:g.5586T>C
NG_033087.1:g.4328A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000643460.2:c.492T>C MANE Select ENSP00000494260.2:p.Tyr164=
ENST00000343060.4:c.492T>C ENSP00000343246.4:p.Tyr164=
ENST00000355633.5:c.355-66T>C ENSP00000347851.5:n.355-66T>C
NM_005522.4:c.492T>C NP_005513.1:p.Tyr164=
NM_153620.2:c.355-66T>C NP_705873.2:n.355-66T>C
NM_005522.5:c.492T>C MANE Select NP_005513.2:p.Tyr164=
NM_153620.3:c.355-66T>C NP_705873.3:n.355-66T>C
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