Canonical Allele Identifier: CA374981521

Gene: ENG

Linked Data

• dbSNP Id: rs1229006135
• gnomAD v2: 9-130586660-C-G
• gnomAD v4: 9-127824381-C-G
• MyVariant Identifiers: chr9:g.130586660C>G (hg19) ; chr9:g.127824381C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127824381C>G , CM000671.2:g.127824381C>G	GRCh38
NC_000009.11:g.130586660C>G , CM000671.1:g.130586660C>G	GRCh37
NC_000009.10:g.129626481C>G	NCBI36
NG_009551.1:g.35388G>C , LRG_589:g.35388G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000480266.6:c.511G>C	ENSP00000479015.1:p.Glu171Gln
ENST00000373203.9:c.1057G>C MANE Select	ENSP00000362299.4:p.Glu353Gln
ENST00000344849.4:c.1057G>C	ENSP00000341917.3:p.Glu353Gln
ENST00000373203.8:c.1057G>C	ENSP00000362299.4:p.Glu353Gln
ENST00000480266.5:c.511G>C	ENSP00000479015.1:p.Glu171Gln
ENST00000486329.1:n.25G>C
NM_000118.3:c.1057G>C , LRG_589t1:c.1057G>C	NP_000109.1:p.Glu353Gln
NM_001114753.2:c.1057G>C , LRG_589t2:c.1057G>C	NP_001108225.1:p.Glu353Gln
NM_001278138.1:c.511G>C	NP_001265067.1:p.Glu171Gln
NM_001114753.3:c.1057G>C MANE Select	NP_001108225.1:p.Glu353Gln
NM_001278138.2:c.511G>C	NP_001265067.1:p.Glu171Gln