Canonical Allele Identifier: CA454507602
Gene: HOXA1 HGNC NCBI

Linked Data

dbSNP Id: rs1393589667
gnomAD v3: 7-27095607-C-T
gnomAD v4: 7-27095607-C-T
MyVariant Identifiers: chr7:g.27135226C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27095607C>T , CM000669.2:g.27095607C>T GRCh38
NC_000007.13:g.27135226C>T , CM000669.1:g.27135226C>T GRCh37
NC_000007.12:g.27101751C>T NCBI36
NG_011813.1:g.5400G>A
NG_033087.1:g.4514C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000643460.2:c.306G>A MANE Select ENSP00000494260.2:p.Gln102=
ENST00000343060.4:c.306G>A ENSP00000343246.4:p.Gln102=
ENST00000355633.5:c.306G>A ENSP00000347851.5:p.Gln102=
NM_005522.4:c.306G>A NP_005513.1:p.Gln102=
NM_153620.2:c.306G>A NP_705873.2:p.Gln102=
NM_005522.5:c.306G>A MANE Select NP_005513.2:p.Gln102=
NM_153620.3:c.306G>A NP_705873.3:p.Gln102=