Canonical Allele Identifier: CA467230895

Gene: ENG

Linked Data

• MyVariant Identifiers: chr9:g.130587086G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127824807G>T , CM000671.2:g.127824807G>T	GRCh38
NC_000009.11:g.130587086G>T , CM000671.1:g.130587086G>T	GRCh37
NC_000009.10:g.129626907G>T	NCBI36
NG_009551.1:g.34962C>A , LRG_589:g.34962C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000480266.6:c.438C>A	ENSP00000479015.1:p.Ser146=
ENST00000373203.9:c.984C>A MANE Select	ENSP00000362299.4:p.Ser328=
ENST00000344849.4:c.984C>A	ENSP00000341917.3:p.Ser328=
ENST00000373203.8:c.984C>A	ENSP00000362299.4:p.Ser328=
ENST00000480266.5:c.438C>A	ENSP00000479015.1:p.Ser146=
NM_000118.3:c.984C>A , LRG_589t1:c.984C>A	NP_000109.1:p.Ser328=
NM_001114753.2:c.984C>A , LRG_589t2:c.984C>A	NP_001108225.1:p.Ser328=
NM_001278138.1:c.438C>A	NP_001265067.1:p.Ser146=
NM_001114753.3:c.984C>A MANE Select	NP_001108225.1:p.Ser328=
NM_001278138.2:c.438C>A	NP_001265067.1:p.Ser146=