Canonical Allele Identifier: CA658683089

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43949961_43949962insCC , CM000685.2:g.43949961_43949962insCC GRCh38
NC_000023.10:g.43809207_43809208insCC , CM000685.1:g.43809207_43809208insCC GRCh37
NC_000023.9:g.43694151_43694152insCC NCBI36
NG_009832.1:g.28715_28716insGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000642620.1:c.240_241insGG (NDP) MANE Select ENSP00000495972.1:p.Phe81GlyfsTer24
ENST00000647044.1:c.240_241insGG (NDP) ENSP00000495811.1:p.Phe81GlyfsTer24
ENST00000378062.5:c.240_241insGG (NDP) ENSP00000367301.5:p.Phe81GlyfsTer24
ENST00000470584.1:n.284_285insGG (NDP)
NM_000266.3:c.240_241insGG (NDP) NP_000257.1:p.Phe81GlyfsTer24
NR_046631.1:n.230_231insCC (NDP-AS1)
NM_000266.4:c.240_241insGG (NDP) MANE Select NP_000257.1:p.Phe81GlyfsTer24