Canonical Allele Identifier: CA374985634

Gene: ENG

Linked Data

• dbSNP Id: rs863223533
• gnomAD v2: 9-130591967-T-A
• gnomAD v3: 9-127829688-T-A
• gnomAD v4: 9-127829688-T-A
• MyVariant Identifiers: chr9:g.130591967T>A (hg19) ; chr9:g.127829688T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127829688T>A , CM000671.2:g.127829688T>A	GRCh38
NC_000009.11:g.130591967T>A , CM000671.1:g.130591967T>A	GRCh37
NC_000009.10:g.129631788T>A	NCBI36
NG_009551.1:g.30081A>T , LRG_589:g.30081A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000480266.6:c.-188A>T	ENSP00000479015.1:n.-188A>T
ENST00000373203.9:c.359A>T MANE Select	ENSP00000362299.4:p.Tyr120Phe
ENST00000344849.4:c.359A>T	ENSP00000341917.3:p.Tyr120Phe
ENST00000373203.8:c.359A>T	ENSP00000362299.4:p.Tyr120Phe
ENST00000462196.1:n.117A>T
ENST00000480266.5:c.-188A>T	ENSP00000479015.1:n.-188A>T
NM_000118.3:c.359A>T , LRG_589t1:c.359A>T	NP_000109.1:p.Tyr120Phe
NM_001114753.2:c.359A>T , LRG_589t2:c.359A>T	NP_001108225.1:p.Tyr120Phe
NM_001278138.1:c.-188A>T	NP_001265067.1:n.-188A>T
XR_001746952.2:n.83-2710T>A
NM_001114753.3:c.359A>T MANE Select	NP_001108225.1:p.Tyr120Phe
NM_001278138.2:c.-188A>T	NP_001265067.1:n.-188A>T