Canonical Allele Identifier: CA2576309605
Gene: HOXB13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.48728231_48728259del , CM000679.2:g.48728231_48728259del GRCh38
NC_000017.10:g.46805593_46805621del , CM000679.1:g.46805593_46805621del GRCh37
NC_000017.9:g.44160592_44160620del NCBI36
NG_033789.1:g.5493_5521del , LRG_771:g.5493_5521del

Transcript Alleles

HGVS Amino-acid change
ENST00000290295.8:c.337_365del MANE Select ENSP00000290295.8:p.Thr113ProfsTer4
ENST00000290295.7:c.337_365del ENSP00000290295.7:p.Thr113ProfsTer4
NM_006361.5:c.337_365del , LRG_771t1:c.337_365del NP_006352.2:p.Thr113ProfsTer4
NM_006361.6:c.337_365del MANE Select NP_006352.2:p.Thr113ProfsTer4