Canonical Allele Identifier: CA374978558

Gene: ENG

Linked Data

• ClinVar Variation Id: 1000011
• ClinVar RCV Id: RCV001296084
• dbSNP Id: rs1315317848
• gnomAD v2: 9-130582256-T-C
• gnomAD v4: 9-127819977-T-C
• MyVariant Identifiers: chr9:g.130582256T>C (hg19) ; chr9:g.127819977T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127819977T>C , CM000671.2:g.127819977T>C	GRCh38
NC_000009.11:g.130582256T>C , CM000671.1:g.130582256T>C	GRCh37
NC_000009.10:g.129622077T>C	NCBI36
NG_009551.1:g.39792A>G , LRG_589:g.39792A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000480266.6:c.649A>G	ENSP00000479015.1:p.Arg217Gly
ENST00000373203.9:c.1195A>G MANE Select	ENSP00000362299.4:p.Arg399Gly
ENST00000344849.4:c.1195A>G	ENSP00000341917.3:p.Arg399Gly
ENST00000373203.8:c.1195A>G	ENSP00000362299.4:p.Arg399Gly
ENST00000480266.5:c.649A>G	ENSP00000479015.1:p.Arg217Gly
ENST00000486329.1:n.163A>G
NM_000118.3:c.1195A>G , LRG_589t1:c.1195A>G	NP_000109.1:p.Arg399Gly
NM_001114753.2:c.1195A>G , LRG_589t2:c.1195A>G	NP_001108225.1:p.Arg399Gly
NM_001278138.1:c.649A>G	NP_001265067.1:p.Arg217Gly
NR_136302.1:n.1569-1218T>C
NM_001114753.3:c.1195A>G MANE Select	NP_001108225.1:p.Arg399Gly
NM_001278138.2:c.649A>G	NP_001265067.1:p.Arg217Gly