Canonical Allele Identifier: CA1696187213
Gene: HOXA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27095689_27095698delinsGGGTGGCGAT , CM000669.2:g.27095689_27095698delinsGGGTGGCGAT GRCh38
NC_000007.13:g.27135308_27135317delinsGGGTGGCGAT , CM000669.1:g.27135308_27135317delinsGGGTGGCGAT GRCh37
NC_000007.12:g.27101833_27101842delinsGGGTGGCGAT NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000643460.2:c.215_224delinsATCGCCACCC MANE Select ENSP00000494260.2:p.His72=
ENST00000343060.4:c.215_224delinsATCGCCACCC ENSP00000343246.4:p.His72=
ENST00000355633.5:c.215_224delinsATCGCCACCC ENSP00000347851.5:p.His72=
NM_005522.5:c.215_224delinsATCGCCACCC MANE Select NP_005513.2:p.His72=
NM_153620.3:c.215_224delinsATCGCCACCC NP_705873.3:p.His72=