Canonical Allele Identifier: CA1146252143

Gene: PTPN14

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214501608T= , CM000663.2:g.214501608T=	GRCh38
NC_000001.10:g.214674951T= , CM000663.1:g.214674951T=	GRCh37
NC_000001.9:g.212741574T=	NCBI36
NG_028036.1:g.55074A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366956.10:c.-154-36651A= MANE Select	ENSP00000355923.4:n.-154-36651A=
ENST00000366956.9:c.-154-36651A=	ENSP00000355923.4:n.-154-36651A=
ENST00000486173.1:n.232-36651A=
ENST00000543945.5:c.-154-36651A=	ENSP00000443330.1:n.-154-36651A=
NM_005401.4:c.-154-36651A=	NP_005392.2:n.-154-36651A=
XR_247032.3:n.421-36651A=
XM_017001941.1:c.-155+31709A=	XP_016857430.1:n.-155+31709A=
XM_024448759.1:c.-155+30856A=	XP_024304527.1:n.-155+30856A=
NM_005401.5:c.-154-36651A= MANE Select	NP_005392.2:n.-154-36651A=