Canonical Allele Identifier: CA374981726

Gene: ENG

Linked Data

• MyVariant Identifiers: chr9:g.130586698G>T (hg19) ; chr9:g.127824419G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127824419G>T , CM000671.2:g.127824419G>T	GRCh38
NC_000009.11:g.130586698G>T , CM000671.1:g.130586698G>T	GRCh37
NC_000009.10:g.129626519G>T	NCBI36
NG_009551.1:g.35350C>A , LRG_589:g.35350C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.473C>A	ENSP00000479015.1:p.Pro158Gln
ENST00000373203.9:c.1019C>A MANE Select	ENSP00000362299.4:p.Pro340Gln
ENST00000344849.4:c.1019C>A	ENSP00000341917.3:p.Pro340Gln
ENST00000373203.8:c.1019C>A	ENSP00000362299.4:p.Pro340Gln
ENST00000480266.5:c.473C>A	ENSP00000479015.1:p.Pro158Gln
NM_000118.3:c.1019C>A , LRG_589t1:c.1019C>A	NP_000109.1:p.Pro340Gln
NM_001114753.2:c.1019C>A , LRG_589t2:c.1019C>A	NP_001108225.1:p.Pro340Gln
NM_001278138.1:c.473C>A	NP_001265067.1:p.Pro158Gln
NM_001114753.3:c.1019C>A MANE Select	NP_001108225.1:p.Pro340Gln
NM_001278138.2:c.473C>A	NP_001265067.1:p.Pro158Gln