Canonical Allele Identifier: CA1879995077
Gene: ENG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127840084_127840085delinsCA , CM000671.2:g.127840084_127840085delinsCA GRCh38
NC_000009.11:g.130602363_130602364delinsCA , CM000671.1:g.130602363_130602364delinsCA GRCh37
NC_000009.10:g.129642184_129642185delinsCA NCBI36
NG_009551.1:g.19684_19685delinsTG , LRG_589:g.19684_19685delinsTG

Transcript Alleles

HGVS Amino-acid change
ENST00000480266.6:c.-328+3009_-328+3010delinsTG ENSP00000479015.1:n.-328+3009_-328+3010de...
ENST00000373203.9:c.219+3009_219+3010delinsTG MANE Select ENSP00000362299.4:n.219+3009_219+3010deli...
ENST00000344849.4:c.219+3009_219+3010delinsTG ENSP00000341917.3:n.219+3009_219+3010deli...
ENST00000373203.8:c.219+3009_219+3010delinsTG ENSP00000362299.4:n.219+3009_219+3010deli...
ENST00000480266.5:c.-328+3009_-328+3010delinsTG ENSP00000479015.1:n.-328+3009_-328+3010de...
NM_000118.3:c.219+3009_219+3010delinsTG , LRG_589t1:c.219+3009_219+3010delinsTG NP_000109.1:n.219+3009_219+3010delinsTG
NM_001114753.2:c.219+3009_219+3010delinsTG , LRG_589t2:c.219+3009_219+3010delinsTG NP_001108225.1:n.219+3009_219+3010delinsT...
NM_001278138.1:c.-328+3009_-328+3010delinsTG NP_001265067.1:n.-328+3009_-328+3010delin...
NM_001114753.3:c.219+3009_219+3010delinsTG MANE Select NP_001108225.1:n.219+3009_219+3010delinsT...
NM_001278138.2:c.-328+3009_-328+3010delinsTG NP_001265067.1:n.-328+3009_-328+3010delin...