Canonical Allele Identifier: CA374970637

Gene: ENG

Linked Data

• MyVariant Identifiers: chr9:g.130578061A>C (hg19) ; chr9:g.127815782A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127815782A>C , CM000671.2:g.127815782A>C	GRCh38
NC_000009.11:g.130578061A>C , CM000671.1:g.130578061A>C	GRCh37
NC_000009.10:g.129617882A>C	NCBI36
NG_009551.1:g.43987T>G , LRG_589:g.43987T>G
NG_023245.1:g.17908A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.1331T>G	ENSP00000479015.1:p.Val444Gly
ENST00000373203.9:c.1877T>G MANE Select	ENSP00000362299.4:p.Val626Gly
ENST00000344849.4:c.*135T>G	ENSP00000341917.3:n.*135T>G
ENST00000373203.8:c.1877T>G	ENSP00000362299.4:p.Val626Gly
ENST00000480266.5:c.1331T>G	ENSP00000479015.1:p.Val444Gly
NM_000118.3:c.*135T>G , LRG_589t1:c.*135T>G	NP_000109.1:n.*135T>G
NM_001114753.2:c.1877T>G , LRG_589t2:c.1877T>G	NP_001108225.1:p.Val626Gly
NM_001278138.1:c.1331T>G	NP_001265067.1:p.Val444Gly
NM_001114753.3:c.1877T>G MANE Select	NP_001108225.1:p.Val626Gly
NM_001278138.2:c.1331T>G	NP_001265067.1:p.Val444Gly