Canonical Allele Identifier: CA367069500
Gene: HOXA1 HGNC NCBI

Linked Data

dbSNP Id: rs1188718334
gnomAD v3: 7-27095784-G-T
gnomAD v4: 7-27095784-G-T
MyVariant Identifiers: chr7:g.27135403G>T (hg19) chr7:g.27095784G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27095784G>T , CM000669.2:g.27095784G>T GRCh38
NC_000007.13:g.27135403G>T , CM000669.1:g.27135403G>T GRCh37
NC_000007.12:g.27101928G>T NCBI36
NG_011813.1:g.5223C>A
NG_033087.1:g.4691G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000643460.2:c.129C>A MANE Select ENSP00000494260.2:p.Ser43Arg
ENST00000343060.4:c.129C>A ENSP00000343246.4:p.Ser43Arg
ENST00000355633.5:c.129C>A ENSP00000347851.5:p.Ser43Arg
NM_005522.4:c.129C>A NP_005513.1:p.Ser43Arg
NM_153620.2:c.129C>A NP_705873.2:p.Ser43Arg
NM_005522.5:c.129C>A MANE Select NP_005513.2:p.Ser43Arg
NM_153620.3:c.129C>A NP_705873.3:p.Ser43Arg
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