Canonical Allele Identifier: CA155901154
Gene: HOXA1 HGNC NCBI

Linked Data

dbSNP Id: rs533892779

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.27095720_27095721insTGGTGGTGG , CM000669.2:g.27095720_27095721insTGGTGGTGG GRCh38
NC_000007.13:g.27135339_27135340insTGGTGGTGG , CM000669.1:g.27135339_27135340insTGGTGGTGG GRCh37
NC_000007.12:g.27101864_27101865insTGGTGGTGG NCBI36
NG_011813.1:g.5287_5288insCACCACCAC
NG_033087.1:g.4627_4628insTGGTGGTGG

Transcript Alleles

HGVS Amino-acid change
ENST00000643460.2:c.193_194insCACCACCAC MANE Select ENSP00000494260.2:p.Pro64_His65insProProP...
ENST00000343060.4:c.193_194insCACCACCAC ENSP00000343246.4:p.Pro64_His65insProProP...
ENST00000355633.5:c.193_194insCACCACCAC ENSP00000347851.5:p.Pro64_His65insProProP...
NM_005522.4:c.193_194insCACCACCAC NP_005513.1:p.Pro64_His65insProProPro
NM_153620.2:c.193_194insCACCACCAC NP_705873.2:p.Pro64_His65insProProPro
NM_005522.5:c.193_194insCACCACCAC MANE Select NP_005513.2:p.Pro64_His65insProProPro
NM_153620.3:c.193_194insCACCACCAC NP_705873.3:p.Pro64_His65insProProPro