Canonical Allele Identifier: CA1879977375

Gene: ENG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127826540G= , CM000671.2:g.127826540G=	GRCh38
NC_000009.11:g.130588819G= , CM000671.1:g.130588819G=	GRCh37
NC_000009.10:g.129628640G=	NCBI36
NG_009551.1:g.33229C= , LRG_589:g.33229C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000480266.6:c.-54C=	ENSP00000479015.1:n.-54C=
ENST00000373203.9:c.493C= MANE Select	ENSP00000362299.4:p.Pro165=
ENST00000344849.4:c.493C=	ENSP00000341917.3:p.Pro165=
ENST00000373203.8:c.493C=	ENSP00000362299.4:p.Pro165=
ENST00000462196.1:n.393C=
ENST00000480266.5:c.-54C=	ENSP00000479015.1:n.-54C=
NM_000118.3:c.493C= , LRG_589t1:c.493C=	NP_000109.1:p.Pro165=
NM_001114753.2:c.493C= , LRG_589t2:c.493C=	NP_001108225.1:p.Pro165=
NM_001278138.1:c.-54C=	NP_001265067.1:n.-54C=
XR_001746952.2:n.82+1082G=
NM_001114753.3:c.493C= MANE Select	NP_001108225.1:p.Pro165=
NM_001278138.2:c.-54C=	NP_001265067.1:n.-54C=