Canonical Allele Identifier: CA1879988810

Gene: ENG

Linked Data

• dbSNP Id: rs1830422479
• gnomAD v4: 9-127819560-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127819560G>A , CM000671.2:g.127819560G>A	GRCh38
NC_000009.11:g.130581839G>A , CM000671.1:g.130581839G>A	GRCh37
NC_000009.10:g.129621660G>A	NCBI36
NG_009551.1:g.40209C>T , LRG_589:g.40209C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.765+62C>T	ENSP00000479015.1:n.765+62C>T
ENST00000373203.9:c.1311+62C>T MANE Select	ENSP00000362299.4:n.1311+62C>T
ENST00000344849.4:c.1311+62C>T	ENSP00000341917.3:n.1311+62C>T
ENST00000373203.8:c.1311+62C>T	ENSP00000362299.4:n.1311+62C>T
ENST00000480266.5:c.765+62C>T	ENSP00000479015.1:n.765+62C>T
ENST00000486329.1:n.341C>T
NM_000118.3:c.1311+62C>T , LRG_589t1:c.1311+62C>T	NP_000109.1:n.1311+62C>T
NM_001114753.2:c.1311+62C>T , LRG_589t2:c.1311+62C>T	NP_001108225.1:n.1311+62C>T
NM_001278138.1:c.765+62C>T	NP_001265067.1:n.765+62C>T
NR_136302.1:n.1568+849G>A
NM_001114753.3:c.1311+62C>T MANE Select	NP_001108225.1:n.1311+62C>T
NM_001278138.2:c.765+62C>T	NP_001265067.1:n.765+62C>T