Canonical Allele Identifier: CA860205107

Gene: ENG

Linked Data

• dbSNP Id: rs555355926
• MyVariant Identifiers: chr9:g.130602560G>T (hg19) ; chr9:g.127840281G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127840281G>T , CM000671.2:g.127840281G>T	GRCh38
NC_000009.11:g.130602560G>T , CM000671.1:g.130602560G>T	GRCh37
NC_000009.10:g.129642381G>T	NCBI36
NG_009551.1:g.19488C>A , LRG_589:g.19488C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.-328+2813C>A	ENSP00000479015.1:n.-328+2813C>A
ENST00000373203.9:c.219+2813C>A MANE Select	ENSP00000362299.4:n.219+2813C>A
ENST00000344849.4:c.219+2813C>A	ENSP00000341917.3:n.219+2813C>A
ENST00000373203.8:c.219+2813C>A	ENSP00000362299.4:n.219+2813C>A
ENST00000480266.5:c.-328+2813C>A	ENSP00000479015.1:n.-328+2813C>A
NM_000118.3:c.219+2813C>A , LRG_589t1:c.219+2813C>A	NP_000109.1:n.219+2813C>A
NM_001114753.2:c.219+2813C>A , LRG_589t2:c.219+2813C>A	NP_001108225.1:n.219+2813C>A
NM_001278138.1:c.-328+2813C>A	NP_001265067.1:n.-328+2813C>A
NM_001114753.3:c.219+2813C>A MANE Select	NP_001108225.1:n.219+2813C>A
NM_001278138.2:c.-328+2813C>A	NP_001265067.1:n.-328+2813C>A