Canonical Allele Identifier: CA1879989529

Gene: ENG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127819892G= , CM000671.2:g.127819892G=	GRCh38
NC_000009.11:g.130582171G= , CM000671.1:g.130582171G=	GRCh37
NC_000009.10:g.129621992G=	NCBI36
NG_009551.1:g.39877C= , LRG_589:g.39877C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000480266.6:c.726+8C=	ENSP00000479015.1:n.726+8C=
ENST00000373203.9:c.1272+8C= MANE Select	ENSP00000362299.4:n.1272+8C=
ENST00000344849.4:c.1272+8C=	ENSP00000341917.3:n.1272+8C=
ENST00000373203.8:c.1272+8C=	ENSP00000362299.4:n.1272+8C=
ENST00000480266.5:c.726+8C=	ENSP00000479015.1:n.726+8C=
ENST00000486329.1:n.240+8C=
NM_000118.3:c.1272+8C= , LRG_589t1:c.1272+8C=	NP_000109.1:n.1272+8C=
NM_001114753.2:c.1272+8C= , LRG_589t2:c.1272+8C=	NP_001108225.1:n.1272+8C=
NM_001278138.1:c.726+8C=	NP_001265067.1:n.726+8C=
NR_136302.1:n.1568+1181G=
NM_001114753.3:c.1272+8C= MANE Select	NP_001108225.1:n.1272+8C=
NM_001278138.2:c.726+8C=	NP_001265067.1:n.726+8C=