Canonical Allele Identifier: CA1879999080
Gene: ENG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127854474G= , CM000671.2:g.127854474G= GRCh38
NC_000009.11:g.130616753G= , CM000671.1:g.130616753G= GRCh37
NC_000009.10:g.129656574G= NCBI36
NG_009551.1:g.5295C= , LRG_589:g.5295C=

Transcript Alleles

HGVS Amino-acid change
ENST00000373203.9:c.-119C= MANE Select ENSP00000362299.4:n.-119C=
ENST00000344849.4:c.-119C= ENSP00000341917.3:n.-119C=
ENST00000373203.8:c.-119C= ENSP00000362299.4:n.-119C=
NM_000118.3:c.-119C= , LRG_589t1:c.-119C= NP_000109.1:n.-119C=
NM_001114753.2:c.-119C= , LRG_589t2:c.-119C= NP_001108225.1:n.-119C=
NM_001114753.3:c.-119C= MANE Select NP_001108225.1:n.-119C=
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