Canonical Allele Identifier: CA374978012

Gene: ENG

Linked Data

• ClinVar Variation Id: 2064062
• ClinVar RCV Id: RCV002943181
• dbSNP Id: rs1830424604
• MyVariant Identifiers: chr9:g.130581912A>T (hg19) ; chr9:g.127819633A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127819633A>T , CM000671.2:g.127819633A>T	GRCh38
NC_000009.11:g.130581912A>T , CM000671.1:g.130581912A>T	GRCh37
NC_000009.10:g.129621733A>T	NCBI36
NG_009551.1:g.40136T>A , LRG_589:g.40136T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000480266.6:c.754T>A	ENSP00000479015.1:p.Ser252Thr
ENST00000373203.9:c.1300T>A MANE Select	ENSP00000362299.4:p.Ser434Thr
ENST00000344849.4:c.1300T>A	ENSP00000341917.3:p.Ser434Thr
ENST00000373203.8:c.1300T>A	ENSP00000362299.4:p.Ser434Thr
ENST00000480266.5:c.754T>A	ENSP00000479015.1:p.Ser252Thr
ENST00000486329.1:n.268T>A
NM_000118.3:c.1300T>A , LRG_589t1:c.1300T>A	NP_000109.1:p.Ser434Thr
NM_001114753.2:c.1300T>A , LRG_589t2:c.1300T>A	NP_001108225.1:p.Ser434Thr
NM_001278138.1:c.754T>A	NP_001265067.1:p.Ser252Thr
NR_136302.1:n.1568+922A>T
NM_001114753.3:c.1300T>A MANE Select	NP_001108225.1:p.Ser434Thr
NM_001278138.2:c.754T>A	NP_001265067.1:p.Ser252Thr