Canonical Allele Identifier: CA2614035276

Gene: SLC22A8

Linked Data

• gnomAD v4: 11-62996078-AC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.62996081del , CM000673.2:g.62996081del	GRCh38
NC_000011.9:g.62763553del , CM000673.1:g.62763553del	GRCh37
NC_000011.8:g.62520129del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336232.7:c.835del MANE Select	ENSP00000337335.2:p.Val279TrpfsTer?
ENST00000311438.12:c.835del	ENSP00000311463.8:p.Val279TrpfsTer?
ENST00000336232.6:c.835del	ENSP00000337335.2:p.Val279TrpfsTer?
ENST00000430500.6:c.835del	ENSP00000398548.2:p.Val279TrpfsTer?
ENST00000535878.5:c.466del	ENSP00000443368.1:p.Val156TrpfsTer?
ENST00000539841.1:n.653del
ENST00000545207.5:c.562del	ENSP00000441658.1:p.Val188TrpfsTer?
NM_001184732.1:c.835del	NP_001171661.1:p.Val279TrpfsTer?
NM_001184733.1:c.562del	NP_001171662.1:p.Val188TrpfsTer?
NM_001184736.1:c.466del	NP_001171665.1:p.Val156TrpfsTer?
NM_004254.3:c.835del	NP_004245.2:p.Val279TrpfsTer?
XM_011545364.1:c.466del	XP_011543666.1:p.Val156TrpfsTer?
NM_004254.4:c.835del MANE Select	NP_004245.2:p.Val279TrpfsTer?
NM_001184732.2:c.835del	NP_001171661.1:p.Val279TrpfsTer?
NM_001184733.2:c.562del	NP_001171662.1:p.Val188TrpfsTer?
NM_001184736.2:c.466del	NP_001171665.1:p.Val156TrpfsTer?