Canonical Allele Identifier: CA4195965
Gene: HOXA1 HGNC NCBI

Linked Data

dbSNP Id: rs372765755
ExAC: 7:27135205 G / A
gnomAD v2: 7-27135205-G-A
MyVariant Identifiers: chr7:g.27135205G>A (hg19) chr7:g.27095586G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27095586G>A , CM000669.2:g.27095586G>A GRCh38
NC_000007.13:g.27135205G>A , CM000669.1:g.27135205G>A GRCh37
NC_000007.12:g.27101730G>A NCBI36
NG_011813.1:g.5421C>T
NG_033087.1:g.4493G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000643460.2:c.327C>T MANE Select ENSP00000494260.2:p.Ser109=
ENST00000343060.4:c.327C>T ENSP00000343246.4:p.Ser109=
ENST00000355633.5:c.327C>T ENSP00000347851.5:p.Ser109=
NM_005522.4:c.327C>T NP_005513.1:p.Ser109=
NM_153620.2:c.327C>T NP_705873.2:p.Ser109=
NM_005522.5:c.327C>T MANE Select NP_005513.2:p.Ser109=
NM_153620.3:c.327C>T NP_705873.3:p.Ser109=
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