Canonical Allele Identifier: CA1879998902
Gene: ENG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127854376T= , CM000671.2:g.127854376T= GRCh38
NC_000009.11:g.130616655T= , CM000671.1:g.130616655T= GRCh37
NC_000009.10:g.129656476T= NCBI36
NG_009551.1:g.5393A= , LRG_589:g.5393A=

Transcript Alleles

HGVS Amino-acid change
ENST00000373203.9:c.-21A= MANE Select ENSP00000362299.4:n.-21A=
ENST00000344849.4:c.-21A= ENSP00000341917.3:n.-21A=
ENST00000373203.8:c.-21A= ENSP00000362299.4:n.-21A=
NM_000118.3:c.-21A= , LRG_589t1:c.-21A= NP_000109.1:n.-21A=
NM_001114753.2:c.-21A= , LRG_589t2:c.-21A= NP_001108225.1:n.-21A=
NM_001114753.3:c.-21A= MANE Select NP_001108225.1:n.-21A=