Canonical Allele Identifier: CA1879980224

Gene: ENG

Linked Data

• dbSNP Id: rs1564450527
• gnomAD v4: 9-127815246-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127815246C>T , CM000671.2:g.127815246C>T	GRCh38
NC_000009.11:g.130577525C>T , CM000671.1:g.130577525C>T	GRCh37
NC_000009.10:g.129617346C>T	NCBI36
NG_009551.1:g.44523G>A , LRG_589:g.44523G>A
NG_023245.1:g.17372C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.*436G>A	ENSP00000479015.1:n.*436G>A
ENST00000373203.9:c.*436G>A MANE Select	ENSP00000362299.4:n.*436G>A
ENST00000344849.4:c.*671G>A	ENSP00000341917.3:n.*671G>A
ENST00000373203.8:c.*436G>A	ENSP00000362299.4:n.*436G>A
ENST00000480266.5:c.*436G>A	ENSP00000479015.1:n.*436G>A
NM_000118.3:c.*671G>A , LRG_589t1:c.*671G>A	NP_000109.1:n.*671G>A
NM_001114753.2:c.*436G>A , LRG_589t2:c.*436G>A	NP_001108225.1:n.*436G>A
NM_001278138.1:c.*436G>A	NP_001265067.1:n.*436G>A
NM_001114753.3:c.*436G>A MANE Select	NP_001108225.1:n.*436G>A
NM_001278138.2:c.*436G>A	NP_001265067.1:n.*436G>A