Canonical Allele Identifier: CA374985946

Gene: ENG

Linked Data

• MyVariant Identifiers: chr9:g.130592017G>T (hg19) ; chr9:g.127829738G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127829738G>T , CM000671.2:g.127829738G>T	GRCh38
NC_000009.11:g.130592017G>T , CM000671.1:g.130592017G>T	GRCh37
NC_000009.10:g.129631838G>T	NCBI36
NG_009551.1:g.30031C>A , LRG_589:g.30031C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.-238C>A	ENSP00000479015.1:n.-238C>A
ENST00000373203.9:c.309C>A MANE Select	ENSP00000362299.4:p.Ser103Arg
ENST00000344849.4:c.309C>A	ENSP00000341917.3:p.Ser103Arg
ENST00000373203.8:c.309C>A	ENSP00000362299.4:p.Ser103Arg
ENST00000462196.1:n.67C>A
ENST00000480266.5:c.-238C>A	ENSP00000479015.1:n.-238C>A
NM_000118.3:c.309C>A , LRG_589t1:c.309C>A	NP_000109.1:p.Ser103Arg
NM_001114753.2:c.309C>A , LRG_589t2:c.309C>A	NP_001108225.1:p.Ser103Arg
NM_001278138.1:c.-238C>A	NP_001265067.1:n.-238C>A
XR_001746952.2:n.83-2660G>T
NM_001114753.3:c.309C>A MANE Select	NP_001108225.1:p.Ser103Arg
NM_001278138.2:c.-238C>A	NP_001265067.1:n.-238C>A