Canonical Allele Identifier: CA367068853
Gene: HOXA1 HGNC NCBI

Linked Data

dbSNP Id: rs1562699791
gnomAD v4: 7-27095599-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27095599C>T , CM000669.2:g.27095599C>T GRCh38
NC_000007.13:g.27135218C>T , CM000669.1:g.27135218C>T GRCh37
NC_000007.12:g.27101743C>T NCBI36
NG_011813.1:g.5408G>A
NG_033087.1:g.4506C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000643460.2:c.314G>A MANE Select ENSP00000494260.2:p.Ser105Asn
ENST00000343060.4:c.314G>A ENSP00000343246.4:p.Ser105Asn
ENST00000355633.5:c.314G>A ENSP00000347851.5:p.Ser105Asn
NM_005522.4:c.314G>A NP_005513.1:p.Ser105Asn
NM_153620.2:c.314G>A NP_705873.2:p.Ser105Asn
NM_005522.5:c.314G>A MANE Select NP_005513.2:p.Ser105Asn
NM_153620.3:c.314G>A NP_705873.3:p.Ser105Asn