Canonical Allele Identifier: CA37570174

Gene: PTPN14

Linked Data

• dbSNP Id: rs1011915809
• MyVariant Identifiers: chr1:g.214501628C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214501628C>G , CM000663.2:g.214501628C>G	GRCh38
NC_000001.10:g.214674971C>G , CM000663.1:g.214674971C>G	GRCh37
NC_000001.9:g.212741594C>G	NCBI36
NG_028036.1:g.55054G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366956.10:c.-154-36671G>C MANE Select	ENSP00000355923.4:n.-154-36671G>C
ENST00000366956.9:c.-154-36671G>C	ENSP00000355923.4:n.-154-36671G>C
ENST00000486173.1:n.232-36671G>C
ENST00000543945.5:c.-154-36671G>C	ENSP00000443330.1:n.-154-36671G>C
NM_005401.4:c.-154-36671G>C	NP_005392.2:n.-154-36671G>C
XR_247032.3:n.421-36671G>C
XM_017001941.1:c.-155+31689G>C	XP_016857430.1:n.-155+31689G>C
XM_024448759.1:c.-155+30836G>C	XP_024304527.1:n.-155+30836G>C
NM_005401.5:c.-154-36671G>C MANE Select	NP_005392.2:n.-154-36671G>C