Canonical Allele Identifier: CA1879981845

Gene: ENG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127829733A= , CM000671.2:g.127829733A=	GRCh38
NC_000009.11:g.130592012A= , CM000671.1:g.130592012A=	GRCh37
NC_000009.10:g.129631833A=	NCBI36
NG_009551.1:g.30036T= , LRG_589:g.30036T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.-233T=	ENSP00000479015.1:n.-233T=
ENST00000373203.9:c.314T= MANE Select	ENSP00000362299.4:p.Val105=
ENST00000344849.4:c.314T=	ENSP00000341917.3:p.Val105=
ENST00000373203.8:c.314T=	ENSP00000362299.4:p.Val105=
ENST00000462196.1:n.72T=
ENST00000480266.5:c.-233T=	ENSP00000479015.1:n.-233T=
NM_000118.3:c.314T= , LRG_589t1:c.314T=	NP_000109.1:p.Val105=
NM_001114753.2:c.314T= , LRG_589t2:c.314T=	NP_001108225.1:p.Val105=
NM_001278138.1:c.-233T=	NP_001265067.1:n.-233T=
XR_001746952.2:n.83-2665A=
NM_001114753.3:c.314T= MANE Select	NP_001108225.1:p.Val105=
NM_001278138.2:c.-233T=	NP_001265067.1:n.-233T=