Canonical Allele Identifier: CA860196696

Gene: ENG

Linked Data

• dbSNP Id: rs1200978018
• gnomAD v3: 9-127824731-T-G
• gnomAD v4: 9-127824731-T-G
• MyVariant Identifiers: chr9:g.130587010T>G (hg19) ; chr9:g.127824731T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127824731T>G , CM000671.2:g.127824731T>G	GRCh38
NC_000009.11:g.130587010T>G , CM000671.1:g.130587010T>G	GRCh37
NC_000009.10:g.129626831T>G	NCBI36
NG_009551.1:g.35038A>C , LRG_589:g.35038A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000480266.6:c.445+69A>C	ENSP00000479015.1:n.445+69A>C
ENST00000373203.9:c.991+69A>C MANE Select	ENSP00000362299.4:n.991+69A>C
ENST00000344849.4:c.991+69A>C	ENSP00000341917.3:n.991+69A>C
ENST00000373203.8:c.991+69A>C	ENSP00000362299.4:n.991+69A>C
ENST00000480266.5:c.445+69A>C	ENSP00000479015.1:n.445+69A>C
NM_000118.3:c.991+69A>C , LRG_589t1:c.991+69A>C	NP_000109.1:n.991+69A>C
NM_001114753.2:c.991+69A>C , LRG_589t2:c.991+69A>C	NP_001108225.1:n.991+69A>C
NM_001278138.1:c.445+69A>C	NP_001265067.1:n.445+69A>C
NM_001114753.3:c.991+69A>C MANE Select	NP_001108225.1:n.991+69A>C
NM_001278138.2:c.445+69A>C	NP_001265067.1:n.445+69A>C