Canonical Allele Identifier: CA1879998372

Gene: ENG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127854078A= , CM000671.2:g.127854078A=	GRCh38
NC_000009.11:g.130616357A= , CM000671.1:g.130616357A=	GRCh37
NC_000009.10:g.129656178A=	NCBI36
NG_009551.1:g.5691T= , LRG_589:g.5691T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373203.9:c.67+211T= MANE Select	ENSP00000362299.4:n.67+211T=
ENST00000344849.4:c.67+211T=	ENSP00000341917.3:n.67+211T=
ENST00000373203.8:c.67+211T=	ENSP00000362299.4:n.67+211T=
NM_000118.3:c.67+211T= , LRG_589t1:c.67+211T=	NP_000109.1:n.67+211T=
NM_001114753.2:c.67+211T= , LRG_589t2:c.67+211T=	NP_001108225.1:n.67+211T=
NM_001114753.3:c.67+211T= MANE Select	NP_001108225.1:n.67+211T=