Canonical Allele Identifier: CA2691805406

Gene: ENG

Linked Data

• gnomAD v4: 9-127815369-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127815369C>G , CM000671.2:g.127815369C>G	GRCh38
NC_000009.11:g.130577648C>G , CM000671.1:g.130577648C>G	GRCh37
NC_000009.10:g.129617469C>G	NCBI36
NG_009551.1:g.44400G>C , LRG_589:g.44400G>C
NG_023245.1:g.17495C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.*313G>C	ENSP00000479015.1:n.*313G>C
ENST00000373203.9:c.*313G>C MANE Select	ENSP00000362299.4:n.*313G>C
ENST00000344849.4:c.*548G>C	ENSP00000341917.3:n.*548G>C
ENST00000373203.8:c.*313G>C	ENSP00000362299.4:n.*313G>C
ENST00000480266.5:c.*313G>C	ENSP00000479015.1:n.*313G>C
NM_000118.3:c.*548G>C , LRG_589t1:c.*548G>C	NP_000109.1:n.*548G>C
NM_001114753.2:c.*313G>C , LRG_589t2:c.*313G>C	NP_001108225.1:n.*313G>C
NM_001278138.1:c.*313G>C	NP_001265067.1:n.*313G>C
NM_001114753.3:c.*313G>C MANE Select	NP_001108225.1:n.*313G>C
NM_001278138.2:c.*313G>C	NP_001265067.1:n.*313G>C