Canonical Allele Identifier: CA5252939

Gene: ENG

Linked Data

• ClinVar Variation Id: 528052
• ClinVar RCV Id: RCV000633132 ; RCV003480724
• dbSNP Id: rs753429934
• ExAC: 9:130587159 C / T
• gnomAD v2: 9-130587159-C-T
• gnomAD v3: 9-127824880-C-T
• gnomAD v4: 9-127824880-C-T
• MyVariant Identifiers: chr9:g.130587159C>T (hg19) ; chr9:g.127824880C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127824880C>T , CM000671.2:g.127824880C>T	GRCh38
NC_000009.11:g.130587159C>T , CM000671.1:g.130587159C>T	GRCh37
NC_000009.10:g.129626980C>T	NCBI36
NG_009551.1:g.34889G>A , LRG_589:g.34889G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.365G>A	ENSP00000479015.1:p.Arg122Gln
ENST00000373203.9:c.911G>A MANE Select	ENSP00000362299.4:p.Arg304Gln
ENST00000344849.4:c.911G>A	ENSP00000341917.3:p.Arg304Gln
ENST00000373203.8:c.911G>A	ENSP00000362299.4:p.Arg304Gln
ENST00000480266.5:c.365G>A	ENSP00000479015.1:p.Arg122Gln
NM_000118.3:c.911G>A , LRG_589t1:c.911G>A	NP_000109.1:p.Arg304Gln
NM_001114753.2:c.911G>A , LRG_589t2:c.911G>A	NP_001108225.1:p.Arg304Gln
NM_001278138.1:c.365G>A	NP_001265067.1:p.Arg122Gln
NM_001114753.3:c.911G>A MANE Select	NP_001108225.1:p.Arg304Gln
NM_001278138.2:c.365G>A	NP_001265067.1:p.Arg122Gln