Canonical Allele Identifier: CA374978587

Gene: ENG

Linked Data

• MyVariant Identifiers: chr9:g.130582261T>A (hg19) ; chr9:g.127819982T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127819982T>A , CM000671.2:g.127819982T>A	GRCh38
NC_000009.11:g.130582261T>A , CM000671.1:g.130582261T>A	GRCh37
NC_000009.10:g.129622082T>A	NCBI36
NG_009551.1:g.39787A>T , LRG_589:g.39787A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000480266.6:c.644A>T	ENSP00000479015.1:p.Glu215Val
ENST00000373203.9:c.1190A>T MANE Select	ENSP00000362299.4:p.Glu397Val
ENST00000344849.4:c.1190A>T	ENSP00000341917.3:p.Glu397Val
ENST00000373203.8:c.1190A>T	ENSP00000362299.4:p.Glu397Val
ENST00000480266.5:c.644A>T	ENSP00000479015.1:p.Glu215Val
ENST00000486329.1:n.158A>T
NM_000118.3:c.1190A>T , LRG_589t1:c.1190A>T	NP_000109.1:p.Glu397Val
NM_001114753.2:c.1190A>T , LRG_589t2:c.1190A>T	NP_001108225.1:p.Glu397Val
NM_001278138.1:c.644A>T	NP_001265067.1:p.Glu215Val
NR_136302.1:n.1569-1213T>A
NM_001114753.3:c.1190A>T MANE Select	NP_001108225.1:p.Glu397Val
NM_001278138.2:c.644A>T	NP_001265067.1:p.Glu215Val