Canonical Allele Identifier: CA2486313678

Gene: PTPN14

Linked Data

• dbSNP Id: rs1654701435

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214501597C>T , CM000663.2:g.214501597C>T	GRCh38
NC_000001.10:g.214674940C>T , CM000663.1:g.214674940C>T	GRCh37
NC_000001.9:g.212741563C>T	NCBI36
NG_028036.1:g.55085G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366956.10:c.-154-36640G>A MANE Select	ENSP00000355923.4:n.-154-36640G>A
ENST00000366956.9:c.-154-36640G>A	ENSP00000355923.4:n.-154-36640G>A
ENST00000486173.1:n.232-36640G>A
ENST00000543945.5:c.-154-36640G>A	ENSP00000443330.1:n.-154-36640G>A
NM_005401.4:c.-154-36640G>A	NP_005392.2:n.-154-36640G>A
XR_247032.3:n.421-36640G>A
XM_017001941.1:c.-155+31720G>A	XP_016857430.1:n.-155+31720G>A
XM_024448759.1:c.-155+30867G>A	XP_024304527.1:n.-155+30867G>A
NM_005401.5:c.-154-36640G>A MANE Select	NP_005392.2:n.-154-36640G>A