Canonical Allele Identifier: CA1879973148

Gene: ENG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127824710C= , CM000671.2:g.127824710C=	GRCh38
NC_000009.11:g.130586989C= , CM000671.1:g.130586989C=	GRCh37
NC_000009.10:g.129626810C=	NCBI36
NG_009551.1:g.35059G= , LRG_589:g.35059G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000480266.6:c.445+90G=	ENSP00000479015.1:n.445+90G=
ENST00000373203.9:c.991+90G= MANE Select	ENSP00000362299.4:n.991+90G=
ENST00000344849.4:c.991+90G=	ENSP00000341917.3:n.991+90G=
ENST00000373203.8:c.991+90G=	ENSP00000362299.4:n.991+90G=
ENST00000480266.5:c.445+90G=	ENSP00000479015.1:n.445+90G=
NM_000118.3:c.991+90G= , LRG_589t1:c.991+90G=	NP_000109.1:n.991+90G=
NM_001114753.2:c.991+90G= , LRG_589t2:c.991+90G=	NP_001108225.1:n.991+90G=
NM_001278138.1:c.445+90G=	NP_001265067.1:n.445+90G=
NM_001114753.3:c.991+90G= MANE Select	NP_001108225.1:n.991+90G=
NM_001278138.2:c.445+90G=	NP_001265067.1:n.445+90G=