Canonical Allele Identifier: CA454507843
Gene: HOXA1 HGNC NCBI

Linked Data

dbSNP Id: rs1455017547
gnomAD v2: 7-27135364-G-A
gnomAD v4: 7-27095745-G-A
MyVariant Identifiers: chr7:g.27135364G>A (hg19) chr7:g.27095745G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27095745G>A , CM000669.2:g.27095745G>A GRCh38
NC_000007.13:g.27135364G>A , CM000669.1:g.27135364G>A GRCh37
NC_000007.12:g.27101889G>A NCBI36
NG_011813.1:g.5262C>T
NG_033087.1:g.4652G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000643460.2:c.168C>T MANE Select ENSP00000494260.2:p.Gly56=
ENST00000343060.4:c.168C>T ENSP00000343246.4:p.Gly56=
ENST00000355633.5:c.168C>T ENSP00000347851.5:p.Gly56=
NM_005522.4:c.168C>T NP_005513.1:p.Gly56=
NM_153620.2:c.168C>T NP_705873.2:p.Gly56=
NM_005522.5:c.168C>T MANE Select NP_005513.2:p.Gly56=
NM_153620.3:c.168C>T NP_705873.3:p.Gly56=
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