Canonical Allele Identifier: CA10653182

Gene: SLC2A10

Linked Data

• ClinVar Variation Id: 338630
• ClinVar RCV Id: RCV000393439
• dbSNP Id: rs6012025
• gnomAD v2: 20-45364623-C-A
• gnomAD v3: 20-46735984-C-A
• gnomAD v4: 20-46735984-C-A
• MyVariant Identifiers: chr20:g.45364623C>A (hg19) ; chr20:g.46735984C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46735984C>A , CM000682.2:g.46735984C>A	GRCh38
NC_000020.10:g.45364623C>A , CM000682.1:g.45364623C>A	GRCh37
NC_000020.9:g.44798030C>A	NCBI36
NG_016284.1:g.31345C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000359271.4:c.*2150C>A MANE Select	ENSP00000352216.2:n.*2150C>A
ENST00000359271.3:c.*2150C>A	ENSP00000352216.2:n.*2150C>A
NM_030777.3:c.*2150C>A	NP_110404.1:n.*2150C>A
XM_011529060.1:c.*2150C>A	XP_011527362.1:n.*2150C>A
XM_011529061.1:c.*2150C>A	XP_011527363.1:n.*2150C>A
XM_011529062.1:c.*2150C>A	XP_011527364.1:n.*2150C>A
XM_011529065.1:c.*2218C>A	XP_011527367.1:n.*2218C>A
XR_936641.1:n.4024C>A
XM_011529060.2:c.*2150C>A	XP_011527362.1:n.*2150C>A
XM_011529061.2:c.*2150C>A	XP_011527363.1:n.*2150C>A
XM_011529062.2:c.*2150C>A	XP_011527364.1:n.*2150C>A
XM_011529065.2:c.*2218C>A	XP_011527367.1:n.*2218C>A
XM_017028087.2:c.*2218C>A	XP_016883576.1:n.*2218C>A
XR_936641.2:n.4011C>A
NM_030777.4:c.*2150C>A MANE Select	NP_110404.1:n.*2150C>A