Canonical Allele Identifier: CA590939414

Gene: ENG

Linked Data

• dbSNP Id: rs1564455317
• gnomAD v2: 9-130586755-C-G
• gnomAD v4: 9-127824476-C-G
• MyVariant Identifiers: chr9:g.130586755C>G (hg19) ; chr9:g.127824476C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127824476C>G , CM000671.2:g.127824476C>G	GRCh38
NC_000009.11:g.130586755C>G , CM000671.1:g.130586755C>G	GRCh37
NC_000009.10:g.129626576C>G	NCBI36
NG_009551.1:g.35293G>C , LRG_589:g.35293G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480266.6:c.446-30G>C	ENSP00000479015.1:n.446-30G>C
ENST00000373203.9:c.992-30G>C MANE Select	ENSP00000362299.4:n.992-30G>C
ENST00000344849.4:c.992-30G>C	ENSP00000341917.3:n.992-30G>C
ENST00000373203.8:c.992-30G>C	ENSP00000362299.4:n.992-30G>C
ENST00000480266.5:c.446-30G>C	ENSP00000479015.1:n.446-30G>C
NM_000118.3:c.992-30G>C , LRG_589t1:c.992-30G>C	NP_000109.1:n.992-30G>C
NM_001114753.2:c.992-30G>C , LRG_589t2:c.992-30G>C	NP_001108225.1:n.992-30G>C
NM_001278138.1:c.446-30G>C	NP_001265067.1:n.446-30G>C
NM_001114753.3:c.992-30G>C MANE Select	NP_001108225.1:n.992-30G>C
NM_001278138.2:c.446-30G>C	NP_001265067.1:n.446-30G>C