Canonical Allele Identifier: CA374984154

Gene: ENG

Linked Data

• gnomAD v4: 9-127826540-G-T
• MyVariant Identifiers: chr9:g.130588819G>T (hg19) ; chr9:g.127826540G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127826540G>T , CM000671.2:g.127826540G>T	GRCh38
NC_000009.11:g.130588819G>T , CM000671.1:g.130588819G>T	GRCh37
NC_000009.10:g.129628640G>T	NCBI36
NG_009551.1:g.33229C>A , LRG_589:g.33229C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000480266.6:c.-54C>A	ENSP00000479015.1:n.-54C>A
ENST00000373203.9:c.493C>A MANE Select	ENSP00000362299.4:p.Pro165Thr
ENST00000344849.4:c.493C>A	ENSP00000341917.3:p.Pro165Thr
ENST00000373203.8:c.493C>A	ENSP00000362299.4:p.Pro165Thr
ENST00000462196.1:n.393C>A
ENST00000480266.5:c.-54C>A	ENSP00000479015.1:n.-54C>A
NM_000118.3:c.493C>A , LRG_589t1:c.493C>A	NP_000109.1:p.Pro165Thr
NM_001114753.2:c.493C>A , LRG_589t2:c.493C>A	NP_001108225.1:p.Pro165Thr
NM_001278138.1:c.-54C>A	NP_001265067.1:n.-54C>A
XR_001746952.2:n.82+1082G>T
NM_001114753.3:c.493C>A MANE Select	NP_001108225.1:p.Pro165Thr
NM_001278138.2:c.-54C>A	NP_001265067.1:n.-54C>A