Canonical Allele Identifier: CA1024368

Gene: SLC22A15

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.116031454C>T , CM000663.2:g.116031454C>T	GRCh38
NC_000001.10:g.116574075C>T , CM000663.1:g.116574075C>T	GRCh37
NC_000001.9:g.116375598C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_018420.3:c.817C>T MANE Select	NP_060890.2:p.Arg273Cys
ENST00000369503.9:c.817C>T MANE Select	ENSP00000358515.4:p.Arg273Cys
NM_018420.2:c.817C>T	NP_060890.2:p.Arg273Cys
ENST00000369502.1:c.*42C>T	ENSP00000358514.1:n.*42C>T
ENST00000369503.8:c.817C>T	ENSP00000358515.4:p.Arg273Cys
XM_005271004.2:c.817C>T	XP_005271061.1:p.Arg273Cys
XM_005271004.3:c.817C>T	XP_005271061.1:p.Arg273Cys
XM_005271005.2:c.124C>T	XP_005271062.1:p.Arg42Cys
XM_005271006.2:c.*42C>T	XP_005271063.1:n.*42C>T
XM_006710753.2:c.604C>T	XP_006710816.1:p.Arg202Cys
XM_006710754.2:c.121C>T	XP_006710817.1:p.Arg41Cys
XM_011541749.1:c.667C>T	XP_011540051.1:p.Arg223Cys
XM_011541750.1:c.544C>T	XP_011540052.1:p.Arg182Cys
XM_011541751.1:c.817C>T	XP_011540053.1:p.Arg273Cys
XM_011541752.1:c.817C>T	XP_011540054.1:p.Arg273Cys
XM_011541753.1:c.817C>T	XP_011540055.1:p.Arg273Cys
XM_024448238.1:c.817C>T	XP_024304006.1:p.Arg273Cys
XM_024448239.1:c.817C>T	XP_024304007.1:p.Arg273Cys
XR_002957027.1:n.908C>T
XR_002957029.1:n.908C>T
XR_002957030.1:n.908C>T
XR_002957031.1:n.908C>T
XR_002957032.1:n.908C>T
XR_002957033.1:n.908C>T
XR_002957034.1:n.908C>T
XR_002957035.1:n.908C>T
XR_426619.2:n.896C>T
XR_426620.2:n.896C>T
XR_426622.2:n.896C>T
XR_946700.1:n.896C>T
XR_946701.1:n.896C>T
XR_946702.1:n.896C>T
XR_946703.1:n.896C>T
XR_946704.1:n.896C>T
XR_946705.1:n.896C>T