Canonical Allele Identifier: CA1696186999
Gene: HOXA1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27095554C= , CM000669.2:g.27095554C= GRCh38
NC_000007.13:g.27135173C= , CM000669.1:g.27135173C= GRCh37
NC_000007.12:g.27101698C= NCBI36
NG_011813.1:g.5453G=
NG_033087.1:g.4461C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000643460.2:c.359G= MANE Select ENSP00000494260.2:p.Ser120=
ENST00000343060.4:c.359G= ENSP00000343246.4:p.Ser120=
ENST00000355633.5:c.354+5G= ENSP00000347851.5:n.354+5G=
NM_005522.4:c.359G= NP_005513.1:p.Ser120=
NM_153620.2:c.354+5G= NP_705873.2:n.354+5G=
NM_005522.5:c.359G= MANE Select NP_005513.2:p.Ser120=
NM_153620.3:c.354+5G= NP_705873.3:n.354+5G=
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