Canonical Allele Identifier: CA679099421

Gene: SLC22A8

Linked Data

• dbSNP Id: rs1439039372
• gnomAD v3: 11-63003922-G-A
• gnomAD v4: 11-63003922-G-A
• MyVariant Identifiers: chr11:g.62771394G>A (hg19) ; chr11:g.63003922G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.63003922G>A , CM000673.2:g.63003922G>A	GRCh38
NC_000011.9:g.62771394G>A , CM000673.1:g.62771394G>A	GRCh37
NC_000011.8:g.62527970G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000336232.7:c.334-3099C>T MANE Select	ENSP00000337335.2:n.334-3099C>T
ENST00000311438.12:c.334-3099C>T	ENSP00000311463.8:n.334-3099C>T
ENST00000336232.6:c.334-3099C>T	ENSP00000337335.2:n.334-3099C>T
ENST00000430500.6:c.334-3099C>T	ENSP00000398548.2:n.334-3099C>T
ENST00000535878.5:c.-36-3099C>T	ENSP00000443368.1:n.-36-3099C>T
ENST00000545207.5:c.61-3099C>T	ENSP00000441658.1:n.61-3099C>T
NM_001184732.1:c.334-3099C>T	NP_001171661.1:n.334-3099C>T
NM_001184733.1:c.61-3099C>T	NP_001171662.1:n.61-3099C>T
NM_001184736.1:c.-36-3099C>T	NP_001171665.1:n.-36-3099C>T
NM_004254.3:c.334-3099C>T	NP_004245.2:n.334-3099C>T
NM_004254.4:c.334-3099C>T MANE Select	NP_004245.2:n.334-3099C>T
NM_001184732.2:c.334-3099C>T	NP_001171661.1:n.334-3099C>T
NM_001184733.2:c.61-3099C>T	NP_001171662.1:n.61-3099C>T
NM_001184736.2:c.-36-3099C>T	NP_001171665.1:n.-36-3099C>T