Canonical Allele Identifier: CA367068620
Gene: HOXA1 HGNC NCBI

Linked Data

gnomAD v4: 7-27095497-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27095497A>C , CM000669.2:g.27095497A>C GRCh38
NC_000007.13:g.27135116A>C , CM000669.1:g.27135116A>C GRCh37
NC_000007.12:g.27101641A>C NCBI36
NG_011813.1:g.5510T>G
NG_033087.1:g.4404A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000643460.2:c.416T>G MANE Select ENSP00000494260.2:p.Met139Arg
ENST00000343060.4:c.416T>G ENSP00000343246.4:p.Met139Arg
ENST00000355633.5:c.354+62T>G ENSP00000347851.5:n.354+62T>G
NM_005522.4:c.416T>G NP_005513.1:p.Met139Arg
NM_153620.2:c.354+62T>G NP_705873.2:n.354+62T>G
NM_005522.5:c.416T>G MANE Select NP_005513.2:p.Met139Arg
NM_153620.3:c.354+62T>G NP_705873.3:n.354+62T>G