Canonical Allele Identifier: CA374983448

Gene: ENG

Linked Data

• gnomAD v4: 9-127825344-T-C
• MyVariant Identifiers: chr9:g.130587623T>C (hg19) ; chr9:g.127825344T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127825344T>C , CM000671.2:g.127825344T>C	GRCh38
NC_000009.11:g.130587623T>C , CM000671.1:g.130587623T>C	GRCh37
NC_000009.10:g.129627444T>C	NCBI36
NG_009551.1:g.34425A>G , LRG_589:g.34425A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.157A>G	ENSP00000479015.1:p.Thr53Ala
ENST00000373203.9:c.703A>G MANE Select	ENSP00000362299.4:p.Thr235Ala
ENST00000344849.4:c.703A>G	ENSP00000341917.3:p.Thr235Ala
ENST00000373203.8:c.703A>G	ENSP00000362299.4:p.Thr235Ala
ENST00000480266.5:c.157A>G	ENSP00000479015.1:p.Thr53Ala
NM_000118.3:c.703A>G , LRG_589t1:c.703A>G	NP_000109.1:p.Thr235Ala
NM_001114753.2:c.703A>G , LRG_589t2:c.703A>G	NP_001108225.1:p.Thr235Ala
NM_001278138.1:c.157A>G	NP_001265067.1:p.Thr53Ala
NM_001114753.3:c.703A>G MANE Select	NP_001108225.1:p.Thr235Ala
NM_001278138.2:c.157A>G	NP_001265067.1:p.Thr53Ala