Canonical Allele Identifier: CA1473999101

Gene: PTPN13

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.86769845A= , CM000666.2:g.86769845A=	GRCh38
NC_000004.11:g.87690998A= , CM000666.1:g.87690998A=	GRCh37
NC_000004.10:g.87910022A=	NCBI36
NG_029704.1:g.180531A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411767.7:c.4566A= MANE Select	ENSP00000407249.2:p.Ile1522=
ENST00000316707.10:c.3993A=	ENSP00000322675.6:p.Ile1331=
ENST00000411767.6:c.4566A=	ENSP00000407249.2:p.Ile1522=
ENST00000427191.6:c.4509A=	ENSP00000408368.2:p.Ile1503=
ENST00000436978.5:c.4581A=	ENSP00000394794.1:p.Ile1527=
ENST00000511467.1:c.4581A=	ENSP00000426626.1:p.Ile1527=
NM_006264.2:c.4509A=	NP_006255.1:p.Ile1503=
NM_080683.2:c.4566A=	NP_542414.1:p.Ile1522=
NM_080684.2:c.3993A=	NP_542415.1:p.Ile1331=
NM_080685.2:c.4581A=	NP_542416.1:p.Ile1527=
XM_005263167.1:c.4584A=	XP_005263224.1:p.Ile1528=
XM_011532163.1:c.4599A=	XP_011530465.1:p.Ile1533=
XM_011532164.1:c.4584A=	XP_011530466.1:p.Ile1528=
XM_011532165.1:c.4581A=	XP_011530467.1:p.Ile1527=
XM_011532166.1:c.4599A=	XP_011530468.1:p.Ile1533=
XM_011532167.1:c.4542A=	XP_011530469.1:p.Ile1514=
XM_011532168.1:c.4599A=	XP_011530470.1:p.Ile1533=
XM_011532169.1:c.4527A=	XP_011530471.1:p.Ile1509=
XM_011532170.1:c.4038A=	XP_011530472.1:p.Ile1346=
XM_011532171.1:c.4026A=	XP_011530473.1:p.Ile1342=
XM_011532172.1:c.4011A=	XP_011530474.1:p.Ile1337=
XM_011532165.2:c.4581A=	XP_011530467.1:p.Ile1527=
XM_017008511.2:c.4566A=	XP_016864000.1:p.Ile1522=
XM_017008512.2:c.4524A=	XP_016864001.1:p.Ile1508=
XM_017008513.2:c.4509A=	XP_016864002.1:p.Ile1503=
XM_017008514.2:c.4524A=	XP_016864003.1:p.Ile1508=
XM_017008515.2:c.4020A=	XP_016864004.1:p.Ile1340=
XM_017008516.2:c.4008A=	XP_016864005.1:p.Ile1336=
NM_080683.3:c.4566A= MANE Select	NP_542414.1:p.Ile1522=
NM_006264.3:c.4509A=	NP_006255.1:p.Ile1503=
NM_080684.3:c.3993A=	NP_542415.1:p.Ile1331=
NM_080685.3:c.4581A=	NP_542416.1:p.Ile1527=