Canonical Allele Identifier: CA4195948
Gene: HOXA1 HGNC NCBI

Linked Data

dbSNP Id: rs774552234
gnomAD v2: 7-27135124-T-G
gnomAD v3: 7-27095505-T-G
gnomAD v4: 7-27095505-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27095505T>G , CM000669.2:g.27095505T>G GRCh38
NC_000007.13:g.27135124T>G , CM000669.1:g.27135124T>G GRCh37
NC_000007.12:g.27101649T>G NCBI36
NG_011813.1:g.5502A>C
NG_033087.1:g.4412T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000643460.2:c.408A>C MANE Select ENSP00000494260.2:p.Ser136=
ENST00000343060.4:c.408A>C ENSP00000343246.4:p.Ser136=
ENST00000355633.5:c.354+54A>C ENSP00000347851.5:n.354+54A>C
NM_005522.4:c.408A>C NP_005513.1:p.Ser136=
NM_153620.2:c.354+54A>C NP_705873.2:n.354+54A>C
NM_005522.5:c.408A>C MANE Select NP_005513.2:p.Ser136=
NM_153620.3:c.354+54A>C NP_705873.3:n.354+54A>C