Canonical Allele Identifier: CA1879995164
Gene: ENG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127840159A= , CM000671.2:g.127840159A= GRCh38
NC_000009.11:g.130602438A= , CM000671.1:g.130602438A= GRCh37
NC_000009.10:g.129642259A= NCBI36
NG_009551.1:g.19610T= , LRG_589:g.19610T=

Transcript Alleles

HGVS Amino-acid change
ENST00000480266.6:c.-328+2935T= ENSP00000479015.1:n.-328+2935T=
ENST00000373203.9:c.219+2935T= MANE Select ENSP00000362299.4:n.219+2935T=
ENST00000344849.4:c.219+2935T= ENSP00000341917.3:n.219+2935T=
ENST00000373203.8:c.219+2935T= ENSP00000362299.4:n.219+2935T=
ENST00000480266.5:c.-328+2935T= ENSP00000479015.1:n.-328+2935T=
NM_000118.3:c.219+2935T= , LRG_589t1:c.219+2935T= NP_000109.1:n.219+2935T=
NM_001114753.2:c.219+2935T= , LRG_589t2:c.219+2935T= NP_001108225.1:n.219+2935T=
NM_001278138.1:c.-328+2935T= NP_001265067.1:n.-328+2935T=
NM_001114753.3:c.219+2935T= MANE Select NP_001108225.1:n.219+2935T=
NM_001278138.2:c.-328+2935T= NP_001265067.1:n.-328+2935T=
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