Canonical Allele Identifier: CA1129279221

Gene: ENG

Linked Data

• dbSNP Id: rs2032941915
• gnomAD v3: 9-127824478-G-A
• gnomAD v4: 9-127824478-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127824478G>A , CM000671.2:g.127824478G>A	GRCh38
NC_000009.11:g.130586757G>A , CM000671.1:g.130586757G>A	GRCh37
NC_000009.10:g.129626578G>A	NCBI36
NG_009551.1:g.35291C>T , LRG_589:g.35291C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.446-32C>T	ENSP00000479015.1:n.446-32C>T
ENST00000373203.9:c.992-32C>T MANE Select	ENSP00000362299.4:n.992-32C>T
ENST00000344849.4:c.992-32C>T	ENSP00000341917.3:n.992-32C>T
ENST00000373203.8:c.992-32C>T	ENSP00000362299.4:n.992-32C>T
ENST00000480266.5:c.446-32C>T	ENSP00000479015.1:n.446-32C>T
NM_000118.3:c.992-32C>T , LRG_589t1:c.992-32C>T	NP_000109.1:n.992-32C>T
NM_001114753.2:c.992-32C>T , LRG_589t2:c.992-32C>T	NP_001108225.1:n.992-32C>T
NM_001278138.1:c.446-32C>T	NP_001265067.1:n.446-32C>T
NM_001114753.3:c.992-32C>T MANE Select	NP_001108225.1:n.992-32C>T
NM_001278138.2:c.446-32C>T	NP_001265067.1:n.446-32C>T