Canonical Allele Identifier: CA467474738

Gene: ENG

Linked Data

• gnomAD v4: 9-127816083-C-A
• MyVariant Identifiers: chr9:g.130578362C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127816083C>A , CM000671.2:g.127816083C>A	GRCh38
NC_000009.11:g.130578362C>A , CM000671.1:g.130578362C>A	GRCh37
NC_000009.10:g.129618183C>A	NCBI36
NG_009551.1:g.43686G>T , LRG_589:g.43686G>T
NG_023245.1:g.18209C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.1196-30G>T	ENSP00000479015.1:n.1196-30G>T
ENST00000373203.9:c.1742-30G>T MANE Select	ENSP00000362299.4:n.1742-30G>T
ENST00000344849.4:c.1742-30G>T	ENSP00000341917.3:n.1742-30G>T
ENST00000373203.8:c.1742-30G>T	ENSP00000362299.4:n.1742-30G>T
ENST00000480266.5:c.1196-30G>T	ENSP00000479015.1:n.1196-30G>T
NM_000118.3:c.1742-30G>T , LRG_589t1:c.1742-30G>T	NP_000109.1:n.1742-30G>T
NM_001114753.2:c.1742-30G>T , LRG_589t2:c.1742-30G>T	NP_001108225.1:n.1742-30G>T
NM_001278138.1:c.1196-30G>T	NP_001265067.1:n.1196-30G>T
XM_011519273.1:c.-496C>A	XP_011517575.1:n.-496C>A
NR_136302.1:n.18C>A
NM_001114753.3:c.1742-30G>T MANE Select	NP_001108225.1:n.1742-30G>T
NM_001278138.2:c.1196-30G>T	NP_001265067.1:n.1196-30G>T