Canonical Allele Identifier: CA1879999074
Gene: ENG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127854471G= , CM000671.2:g.127854471G= GRCh38
NC_000009.11:g.130616750G= , CM000671.1:g.130616750G= GRCh37
NC_000009.10:g.129656571G= NCBI36
NG_009551.1:g.5298C= , LRG_589:g.5298C=

Transcript Alleles

HGVS Amino-acid change
ENST00000373203.9:c.-116C= MANE Select ENSP00000362299.4:n.-116C=
ENST00000344849.4:c.-116C= ENSP00000341917.3:n.-116C=
ENST00000373203.8:c.-116C= ENSP00000362299.4:n.-116C=
NM_000118.3:c.-116C= , LRG_589t1:c.-116C= NP_000109.1:n.-116C=
NM_001114753.2:c.-116C= , LRG_589t2:c.-116C= NP_001108225.1:n.-116C=
NM_001114753.3:c.-116C= MANE Select NP_001108225.1:n.-116C=
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