Canonical Allele Identifier: CA2486313684

Gene: PTPN14

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214501607_214501613delinsCTCTTTT , CM000663.2:g.214501607_214501613delinsCTCTTTT	GRCh38
NC_000001.10:g.214674950_214674956delinsCTCTTTT , CM000663.1:g.214674950_214674956delinsCTCTTTT	GRCh37
NC_000001.9:g.212741573_212741579delinsCTCTTTT	NCBI36
NG_028036.1:g.55069_55075delinsAAAAGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366956.10:c.-154-36656_-154-36650delinsAAAAGAG MANE Select	ENSP00000355923.4:n.-154-36656_-154-36650delinsAAAAGAG
ENST00000366956.9:c.-154-36656_-154-36650delinsAAAAGAG	ENSP00000355923.4:n.-154-36656_-154-36650delinsAAAAGAG
ENST00000486173.1:n.232-36656_232-36650delinsAAAAGAG
ENST00000543945.5:c.-154-36656_-154-36650delinsAAAAGAG	ENSP00000443330.1:n.-154-36656_-154-36650delinsAAAAGAG
NM_005401.4:c.-154-36656_-154-36650delinsAAAAGAG	NP_005392.2:n.-154-36656_-154-36650delinsAAAAGAG
XR_247032.3:n.421-36656_421-36650delinsAAAAGAG
XM_017001941.1:c.-155+31704_-155+31710delinsAAAAGAG	XP_016857430.1:n.-155+31704_-155+31710delinsAAAAGAG
XM_024448759.1:c.-155+30851_-155+30857delinsAAAAGAG	XP_024304527.1:n.-155+30851_-155+30857delinsAAAAGAG
NM_005401.5:c.-154-36656_-154-36650delinsAAAAGAG MANE Select	NP_005392.2:n.-154-36656_-154-36650delinsAAAAGAG