Canonical Allele Identifier: CA374972338

Gene: ENG

Linked Data

• ClinVar Variation Id: 1013753
• ClinVar RCV Id: RCV001312394
• dbSNP Id: rs1830304920
• MyVariant Identifiers: chr9:g.130578330A>C (hg19) ; chr9:g.127816051A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127816051A>C , CM000671.2:g.127816051A>C	GRCh38
NC_000009.11:g.130578330A>C , CM000671.1:g.130578330A>C	GRCh37
NC_000009.10:g.129618151A>C	NCBI36
NG_009551.1:g.43718T>G , LRG_589:g.43718T>G
NG_023245.1:g.18177A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.1198T>G	ENSP00000479015.1:p.Cys400Gly
ENST00000373203.9:c.1744T>G MANE Select	ENSP00000362299.4:p.Cys582Gly
ENST00000344849.4:c.1744T>G	ENSP00000341917.3:p.Cys582Gly
ENST00000373203.8:c.1744T>G	ENSP00000362299.4:p.Cys582Gly
ENST00000480266.5:c.1198T>G	ENSP00000479015.1:p.Cys400Gly
NM_000118.3:c.1744T>G , LRG_589t1:c.1744T>G	NP_000109.1:p.Cys582Gly
NM_001114753.2:c.1744T>G , LRG_589t2:c.1744T>G	NP_001108225.1:p.Cys582Gly
NM_001278138.1:c.1198T>G	NP_001265067.1:p.Cys400Gly
NM_001114753.3:c.1744T>G MANE Select	NP_001108225.1:p.Cys582Gly
NM_001278138.2:c.1198T>G	NP_001265067.1:p.Cys400Gly