Canonical Allele Identifier: CA374978203

Gene: ENG

Linked Data

• ClinVar Variation Id: 993863
• ClinVar RCV Id: RCV001286024
• dbSNP Id: rs1830431391
• gnomAD v4: 9-127819898-A-G
• MyVariant Identifiers: chr9:g.130582177A>G (hg19) ; chr9:g.127819898A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127819898A>G , CM000671.2:g.127819898A>G	GRCh38
NC_000009.11:g.130582177A>G , CM000671.1:g.130582177A>G	GRCh37
NC_000009.10:g.129621998A>G	NCBI36
NG_009551.1:g.39871T>C , LRG_589:g.39871T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000480266.6:c.726+2T>C	ENSP00000479015.1:n.726+2T>C
ENST00000373203.9:c.1272+2T>C MANE Select	ENSP00000362299.4:n.1272+2T>C
ENST00000344849.4:c.1272+2T>C	ENSP00000341917.3:n.1272+2T>C
ENST00000373203.8:c.1272+2T>C	ENSP00000362299.4:n.1272+2T>C
ENST00000480266.5:c.726+2T>C	ENSP00000479015.1:n.726+2T>C
ENST00000486329.1:n.240+2T>C
NM_000118.3:c.1272+2T>C , LRG_589t1:c.1272+2T>C	NP_000109.1:n.1272+2T>C
NM_001114753.2:c.1272+2T>C , LRG_589t2:c.1272+2T>C	NP_001108225.1:n.1272+2T>C
NM_001278138.1:c.726+2T>C	NP_001265067.1:n.726+2T>C
NR_136302.1:n.1568+1187A>G
NM_001114753.3:c.1272+2T>C MANE Select	NP_001108225.1:n.1272+2T>C
NM_001278138.2:c.726+2T>C	NP_001265067.1:n.726+2T>C