Canonical Allele Identifier: CA590939440

Gene: ENG

Linked Data

• dbSNP Id: rs1370928222
• gnomAD v2: 9-130586984-C-A
• gnomAD v3: 9-127824705-C-A
• gnomAD v4: 9-127824705-C-A
• MyVariant Identifiers: chr9:g.130586984C>A (hg19) ; chr9:g.127824705C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127824705C>A , CM000671.2:g.127824705C>A	GRCh38
NC_000009.11:g.130586984C>A , CM000671.1:g.130586984C>A	GRCh37
NC_000009.10:g.129626805C>A	NCBI36
NG_009551.1:g.35064G>T , LRG_589:g.35064G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000480266.6:c.445+95G>T	ENSP00000479015.1:n.445+95G>T
ENST00000373203.9:c.991+95G>T MANE Select	ENSP00000362299.4:n.991+95G>T
ENST00000344849.4:c.991+95G>T	ENSP00000341917.3:n.991+95G>T
ENST00000373203.8:c.991+95G>T	ENSP00000362299.4:n.991+95G>T
ENST00000480266.5:c.445+95G>T	ENSP00000479015.1:n.445+95G>T
NM_000118.3:c.991+95G>T , LRG_589t1:c.991+95G>T	NP_000109.1:n.991+95G>T
NM_001114753.2:c.991+95G>T , LRG_589t2:c.991+95G>T	NP_001108225.1:n.991+95G>T
NM_001278138.1:c.445+95G>T	NP_001265067.1:n.445+95G>T
NM_001114753.3:c.991+95G>T MANE Select	NP_001108225.1:n.991+95G>T
NM_001278138.2:c.445+95G>T	NP_001265067.1:n.445+95G>T