Canonical Allele Identifier: CA374978468

Gene: ENG

Linked Data

• MyVariant Identifiers: chr9:g.130582240A>T (hg19) ; chr9:g.127819961A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127819961A>T , CM000671.2:g.127819961A>T	GRCh38
NC_000009.11:g.130582240A>T , CM000671.1:g.130582240A>T	GRCh37
NC_000009.10:g.129622061A>T	NCBI36
NG_009551.1:g.39808T>A , LRG_589:g.39808T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.665T>A	ENSP00000479015.1:p.Val222Asp
ENST00000373203.9:c.1211T>A MANE Select	ENSP00000362299.4:p.Val404Asp
ENST00000344849.4:c.1211T>A	ENSP00000341917.3:p.Val404Asp
ENST00000373203.8:c.1211T>A	ENSP00000362299.4:p.Val404Asp
ENST00000480266.5:c.665T>A	ENSP00000479015.1:p.Val222Asp
ENST00000486329.1:n.179T>A
NM_000118.3:c.1211T>A , LRG_589t1:c.1211T>A	NP_000109.1:p.Val404Asp
NM_001114753.2:c.1211T>A , LRG_589t2:c.1211T>A	NP_001108225.1:p.Val404Asp
NM_001278138.1:c.665T>A	NP_001265067.1:p.Val222Asp
NR_136302.1:n.1569-1234A>T
NM_001114753.3:c.1211T>A MANE Select	NP_001108225.1:p.Val404Asp
NM_001278138.2:c.665T>A	NP_001265067.1:p.Val222Asp