Canonical Allele Identifier: CA2486313672

Gene: PTPN14

Linked Data

• dbSNP Id: rs17042140

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214501582T>G , CM000663.2:g.214501582T>G	GRCh38
NC_000001.10:g.214674925T>G , CM000663.1:g.214674925T>G	GRCh37
NC_000001.9:g.212741548T>G	NCBI36
NG_028036.1:g.55100A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000366956.10:c.-154-36625A>C MANE Select	ENSP00000355923.4:n.-154-36625A>C
ENST00000366956.9:c.-154-36625A>C	ENSP00000355923.4:n.-154-36625A>C
ENST00000486173.1:n.232-36625A>C
ENST00000543945.5:c.-154-36625A>C	ENSP00000443330.1:n.-154-36625A>C
NM_005401.4:c.-154-36625A>C	NP_005392.2:n.-154-36625A>C
XR_247032.3:n.421-36625A>C
XM_017001941.1:c.-155+31735A>C	XP_016857430.1:n.-155+31735A>C
XM_024448759.1:c.-155+30882A>C	XP_024304527.1:n.-155+30882A>C
NM_005401.5:c.-154-36625A>C MANE Select	NP_005392.2:n.-154-36625A>C