Canonical Allele Identifier: CA3088990959

Gene: PTPN4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.119882434T= , CM000664.2:g.119882434T=	GRCh38
NC_000002.11:g.120640010T= , CM000664.1:g.120640010T=	GRCh37
NC_000002.10:g.120356480T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_002830.4:c.467-69T= MANE Select	NP_002821.1:n.467-69T=
ENST00000263708.7:c.467-69T= MANE Select	ENSP00000263708.2:n.467-69T=
NM_002830.3:c.467-69T=	NP_002821.1:n.467-69T=
ENST00000263708.6:c.467-69T=	ENSP00000263708.2:n.467-69T=
ENST00000433888.5:c.221-69T=	ENSP00000411364.1:n.221-69T=
ENST00000485247.1:n.514-69T=
XM_011511560.1:c.488-69T=	XP_011509862.1:n.488-69T=
XM_011511560.3:c.488-69T=	XP_011509862.1:n.488-69T=
XM_011511561.1:c.443-69T=	XP_011509863.1:n.443-69T=
XM_011511562.1:c.422-69T=	XP_011509864.1:n.422-69T=
XM_011511562.3:c.422-69T=	XP_011509864.1:n.422-69T=
XM_017004596.2:c.509-69T=	XP_016860085.1:n.509-69T=
XM_017004597.2:c.509-69T=	XP_016860086.1:n.509-69T=
XM_017004598.2:c.488-69T=	XP_016860087.1:n.488-69T=
XM_017004599.2:c.488-69T=	XP_016860088.1:n.488-69T=
XM_017004600.2:c.467-69T=	XP_016860089.1:n.467-69T=
XM_017004601.2:c.464-69T=	XP_016860090.1:n.464-69T=
XM_017004602.2:c.443-69T=	XP_016860091.1:n.443-69T=
XM_017004603.2:c.422-69T=	XP_016860092.1:n.422-69T=
XM_017004604.2:c.-566-69T=	XP_016860093.1:n.-566-69T=
XM_017004605.2:c.-462-69T=	XP_016860094.1:n.-462-69T=
XM_017004606.2:c.-566-69T=	XP_016860095.1:n.-566-69T=
XM_017004607.2:c.-393-69T=	XP_016860096.1:n.-393-69T=
XM_017004608.2:c.-305-69T=	XP_016860097.1:n.-305-69T=
XM_024453028.1:c.-393-69T=	XP_024308796.1:n.-393-69T=
XM_024453029.1:c.-566-69T=	XP_024308797.1:n.-566-69T=
XM_024453030.1:c.-462-69T=	XP_024308798.1:n.-462-69T=