Canonical Allele Identifier: CA1879988706

Gene: ENG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127819520C= , CM000671.2:g.127819520C=	GRCh38
NC_000009.11:g.130581799C= , CM000671.1:g.130581799C=	GRCh37
NC_000009.10:g.129621620C=	NCBI36
NG_009551.1:g.40249G= , LRG_589:g.40249G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.765+102G=	ENSP00000479015.1:n.765+102G=
ENST00000373203.9:c.1311+102G= MANE Select	ENSP00000362299.4:n.1311+102G=
ENST00000344849.4:c.1311+102G=	ENSP00000341917.3:n.1311+102G=
ENST00000373203.8:c.1311+102G=	ENSP00000362299.4:n.1311+102G=
ENST00000480266.5:c.765+102G=	ENSP00000479015.1:n.765+102G=
ENST00000486329.1:n.381G=
NM_000118.3:c.1311+102G= , LRG_589t1:c.1311+102G=	NP_000109.1:n.1311+102G=
NM_001114753.2:c.1311+102G= , LRG_589t2:c.1311+102G=	NP_001108225.1:n.1311+102G=
NM_001278138.1:c.765+102G=	NP_001265067.1:n.765+102G=
NR_136302.1:n.1568+809C=
NM_001114753.3:c.1311+102G= MANE Select	NP_001108225.1:n.1311+102G=
NM_001278138.2:c.765+102G=	NP_001265067.1:n.765+102G=