Canonical Allele Identifier: CA2675573926
Gene: HBEGF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140333372_140333373insCCATAG , CM000667.2:g.140333372_140333373insCCATAG GRCh38
NC_000005.9:g.139712957_139712958insCCATAG , CM000667.1:g.139712957_139712958insCCATAG GRCh37
NC_000005.8:g.139693141_139693142insCCATAG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000230990.7:c.*926_*927insCTATGG MANE Select ENSP00000230990.6:n.*926_*927insCTATGG
ENST00000230990.6:c.*926_*927insCTATGG ENSP00000230990.6:n.*926_*927insCTATGG
NM_001945.2:c.*926_*927insCTATGG NP_001936.1:n.*926_*927insCTATGG
NM_001945.3:c.*926_*927insCTATGG MANE Select NP_001936.1:n.*926_*927insCTATGG