Canonical Allele Identifier: CA1718932047

Gene: PTPN12

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.77618504G= , CM000669.2:g.77618504G=	GRCh38
NC_000007.13:g.77247821G= , CM000669.1:g.77247821G=	GRCh37
NC_000007.12:g.77085757G=	NCBI36
NG_008394.1:g.86049G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248594.11:c.964G= MANE Select	ENSP00000248594.6:p.Val322=
ENST00000248594.10:c.964G=	ENSP00000248594.6:p.Val322=
ENST00000415482.6:c.607G=	ENSP00000392429.2:p.Val203=
ENST00000435495.6:c.574G=	ENSP00000397991.2:p.Val192=
NM_001131008.1:c.607G=	NP_001124480.1:p.Val203=
NM_001131009.1:c.574G=	NP_001124481.1:p.Val192=
NM_002835.3:c.964G=	NP_002826.3:p.Val322=
XM_005250518.1:c.619G=	XP_005250575.1:p.Val207=
XM_006716073.2:c.868G=	XP_006716136.1:p.Val290=
XM_011516444.1:c.325G=	XP_011514746.1:p.Val109=
XM_005250518.2:c.619G=	XP_005250575.1:p.Val207=
XM_006716073.4:c.868G=	XP_006716136.1:p.Val290=
XM_017012474.2:c.619G=	XP_016867963.1:p.Val207=
XR_001744844.2:n.1321G=
NM_002835.4:c.964G= MANE Select	NP_002826.3:p.Val322=
NM_001131008.2:c.607G=	NP_001124480.1:p.Val203=
NM_001131009.2:c.574G=	NP_001124481.1:p.Val192=