Canonical Allele Identifier: CA374976923

Gene: ENG

Linked Data

• gnomAD v4: 9-127818747-G-A
• MyVariant Identifiers: chr9:g.130581026G>A (hg19) ; chr9:g.127818747G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127818747G>A , CM000671.2:g.127818747G>A	GRCh38
NC_000009.11:g.130581026G>A , CM000671.1:g.130581026G>A	GRCh37
NC_000009.10:g.129620847G>A	NCBI36
NG_009551.1:g.41022C>T , LRG_589:g.41022C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000480266.6:c.851C>T	ENSP00000479015.1:p.Thr284Ile
ENST00000373203.9:c.1397C>T MANE Select	ENSP00000362299.4:p.Thr466Ile
ENST00000344849.4:c.1397C>T	ENSP00000341917.3:p.Thr466Ile
ENST00000373203.8:c.1397C>T	ENSP00000362299.4:p.Thr466Ile
ENST00000480266.5:c.851C>T	ENSP00000479015.1:p.Thr284Ile
NM_000118.3:c.1397C>T , LRG_589t1:c.1397C>T	NP_000109.1:p.Thr466Ile
NM_001114753.2:c.1397C>T , LRG_589t2:c.1397C>T	NP_001108225.1:p.Thr466Ile
NM_001278138.1:c.851C>T	NP_001265067.1:p.Thr284Ile
NR_136302.1:n.1568+36G>A
NM_001114753.3:c.1397C>T MANE Select	NP_001108225.1:p.Thr466Ile
NM_001278138.2:c.851C>T	NP_001265067.1:p.Thr284Ile