Canonical Allele Identifier: CA6059842

Gene: SLC22A8

Linked Data

• dbSNP Id: rs780564481
• ExAC: 11:62766368 A / C
• gnomAD v2: 11-62766368-A-C
• gnomAD v3: 11-62998896-A-C
• gnomAD v4: 11-62998896-A-C
• MyVariant Identifiers: chr11:g.62766368A>C (hg19) ; chr11:g.62998896A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62998896A>C , CM000673.2:g.62998896A>C	GRCh38
NC_000011.9:g.62766368A>C , CM000673.1:g.62766368A>C	GRCh37
NC_000011.8:g.62522944A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000336232.7:c.761+25T>G MANE Select	ENSP00000337335.2:n.761+25T>G
ENST00000311438.12:c.761+25T>G	ENSP00000311463.8:n.761+25T>G
ENST00000336232.6:c.761+25T>G	ENSP00000337335.2:n.761+25T>G
ENST00000430500.6:c.761+25T>G	ENSP00000398548.2:n.761+25T>G
ENST00000535878.5:c.392+25T>G	ENSP00000443368.1:n.392+25T>G
ENST00000539841.1:n.579+25T>G
ENST00000542795.5:n.482+25T>G
ENST00000542904.1:n.601+25T>G
ENST00000545207.5:c.488+25T>G	ENSP00000441658.1:n.488+25T>G
NM_001184732.1:c.761+25T>G	NP_001171661.1:n.761+25T>G
NM_001184733.1:c.488+25T>G	NP_001171662.1:n.488+25T>G
NM_001184736.1:c.392+25T>G	NP_001171665.1:n.392+25T>G
NM_004254.3:c.761+25T>G	NP_004245.2:n.761+25T>G
XM_011545364.1:c.392+25T>G	XP_011543666.1:n.392+25T>G
NM_004254.4:c.761+25T>G MANE Select	NP_004245.2:n.761+25T>G
NM_001184732.2:c.761+25T>G	NP_001171661.1:n.761+25T>G
NM_001184733.2:c.488+25T>G	NP_001171662.1:n.488+25T>G
NM_001184736.2:c.392+25T>G	NP_001171665.1:n.392+25T>G