Canonical Allele Identifier: CA343957086

Gene: TPR PRG4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186312841C>G , CM000663.2:g.186312841C>G	GRCh38
NC_000001.10:g.186281973C>G , CM000663.1:g.186281973C>G	GRCh37
NC_000001.9:g.184548596C>G	NCBI36
NG_008248.2:g.21556C>G
NG_023284.1:g.67485G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_003292.3:c.*1130G>C (TPR) MANE Select	NP_003283.2:n.*1130G>C
NM_005807.6:c.4064C>G (PRG4) MANE Select	NP_005798.3:p.Ser1355Ter
ENST00000367478.9:c.*1130G>C (TPR) MANE Select	ENSP00000356448.3:n.*1130G>C
ENST00000445192.7:c.4064C>G (PRG4) MANE Select	ENSP00000399679.3:p.Ser1355Ter
NM_001127708.2:c.3941C>G (PRG4)	NP_001121180.2:p.Ser1314Ter
NM_001127708.3:c.3941C>G (PRG4)	NP_001121180.2:p.Ser1314Ter
NM_001127709.2:c.3785C>G (PRG4)	NP_001121181.2:p.Ser1262Ter
NM_001127709.3:c.3785C>G (PRG4)	NP_001121181.2:p.Ser1262Ter
NM_001127710.2:c.3662C>G (PRG4)	NP_001121182.2:p.Ser1221Ter
NM_001127710.3:c.3662C>G (PRG4)	NP_001121182.2:p.Ser1221Ter
NM_001303232.1:c.3935C>G (PRG4)	NP_001290161.1:p.Ser1312Ter
NM_001303232.2:c.3935C>G (PRG4)	NP_001290161.1:p.Ser1312Ter
NM_003292.2:c.*1130G>C (TPR)	NP_003283.2:n.*1130G>C
NM_005807.4:c.4064C>G (PRG4)	NP_005798.3:p.Ser1355Ter
ENST00000367478.8:c.*1130G>C (TPR)	ENSP00000356448.3:n.*1130G>C
ENST00000367483.8:c.3941C>G (PRG4)	ENSP00000356453.4:p.Ser1314Ter
ENST00000367485.4:c.3785C>G (PRG4)	ENSP00000356455.4:p.Ser1262Ter
ENST00000445192.6:c.4064C>G (PRG4)	ENSP00000399679.2:p.Ser1355Ter
ENST00000635041.1:c.3935C>G (PRG4)	ENSP00000489292.1:p.Ser1312Ter
XM_024448707.1:c.4064C>G (PRG4)	XP_024304475.1:p.Ser1355Ter
XM_024448717.1:c.3941C>G (PRG4)	XP_024304485.1:p.Ser1314Ter