Canonical Allele Identifier: CA1474016198

Gene: PTPN13 SLC10A6

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.86809827C= , CM000666.2:g.86809827C=	GRCh38
NC_000004.11:g.87730980C= , CM000666.1:g.87730980C=	GRCh37
NC_000004.10:g.87950004C=	NCBI36
NG_029704.1:g.220513C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411767.7:c.7142C= (PTPN13) MANE Select	ENSP00000407249.2:p.Thr2381=
ENST00000316707.10:c.6569C= (PTPN13)	ENSP00000322675.6:p.Thr2190=
ENST00000411767.6:c.7142C= (PTPN13)	ENSP00000407249.2:p.Thr2381=
ENST00000427191.6:c.7085C= (PTPN13)	ENSP00000408368.2:p.Thr2362=
ENST00000436978.5:c.7157C= (PTPN13)	ENSP00000394794.1:p.Thr2386=
ENST00000511467.1:c.7157C= (PTPN13)	ENSP00000426626.1:p.Thr2386=
NM_006264.2:c.7085C= (PTPN13)	NP_006255.1:p.Thr2362=
NM_080683.2:c.7142C= (PTPN13)	NP_542414.1:p.Thr2381=
NM_080684.2:c.6569C= (PTPN13)	NP_542415.1:p.Thr2190=
NM_080685.2:c.7157C= (PTPN13)	NP_542416.1:p.Thr2386=
XM_005263167.1:c.7160C= (PTPN13)	XP_005263224.1:p.Thr2387=
XM_011531923.1:c.1038+13957G= (SLC10A6)	XP_011530225.1:n.1038+13957G=
XM_011532163.1:c.7226C= (PTPN13)	XP_011530465.1:p.Thr2409=
XM_011532164.1:c.7211C= (PTPN13)	XP_011530466.1:p.Thr2404=
XM_011532165.1:c.7208C= (PTPN13)	XP_011530467.1:p.Thr2403=
XM_011532166.1:c.7175C= (PTPN13)	XP_011530468.1:p.Thr2392=
XM_011532167.1:c.7169C= (PTPN13)	XP_011530469.1:p.Thr2390=
XM_011532168.1:c.7127C= (PTPN13)	XP_011530470.1:p.Thr2376=
XM_011532169.1:c.7103C= (PTPN13)	XP_011530471.1:p.Thr2368=
XM_011532170.1:c.6665C= (PTPN13)	XP_011530472.1:p.Thr2222=
XM_011532171.1:c.6653C= (PTPN13)	XP_011530473.1:p.Thr2218=
XM_011532172.1:c.6587C= (PTPN13)	XP_011530474.1:p.Thr2196=
XM_011532165.2:c.7208C= (PTPN13)	XP_011530467.1:p.Thr2403=
XM_017008511.2:c.7193C= (PTPN13)	XP_016864000.1:p.Thr2398=
XM_017008512.2:c.7151C= (PTPN13)	XP_016864001.1:p.Thr2384=
XM_017008513.2:c.7136C= (PTPN13)	XP_016864002.1:p.Thr2379=
XM_017008514.2:c.7100C= (PTPN13)	XP_016864003.1:p.Thr2367=
XM_017008515.2:c.6647C= (PTPN13)	XP_016864004.1:p.Thr2216=
XM_017008516.2:c.6635C= (PTPN13)	XP_016864005.1:p.Thr2212=
NM_080683.3:c.7142C= (PTPN13) MANE Select	NP_542414.1:p.Thr2381=
NM_006264.3:c.7085C= (PTPN13)	NP_006255.1:p.Thr2362=
NM_080684.3:c.6569C= (PTPN13)	NP_542415.1:p.Thr2190=
NM_080685.3:c.7157C= (PTPN13)	NP_542416.1:p.Thr2386=