Canonical Allele Identifier: CA367069151
Gene: HOXA1 HGNC NCBI

Linked Data

gnomAD v4: 7-27095689-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27095689G>C , CM000669.2:g.27095689G>C GRCh38
NC_000007.13:g.27135308G>C , CM000669.1:g.27135308G>C GRCh37
NC_000007.12:g.27101833G>C NCBI36
NG_011813.1:g.5318C>G
NG_033087.1:g.4596G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000643460.2:c.224C>G MANE Select ENSP00000494260.2:p.Pro75Arg
ENST00000343060.4:c.224C>G ENSP00000343246.4:p.Pro75Arg
ENST00000355633.5:c.224C>G ENSP00000347851.5:p.Pro75Arg
NM_005522.4:c.224C>G NP_005513.1:p.Pro75Arg
NM_153620.2:c.224C>G NP_705873.2:p.Pro75Arg
NM_005522.5:c.224C>G MANE Select NP_005513.2:p.Pro75Arg
NM_153620.3:c.224C>G NP_705873.3:p.Pro75Arg