Canonical Allele Identifier: CA1296645

Gene: PRG4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186309867C>T , CM000663.2:g.186309867C>T	GRCh38
NC_000001.10:g.186278999C>T , CM000663.1:g.186278999C>T	GRCh37
NC_000001.9:g.184545622C>T	NCBI36
NG_008248.2:g.18582C>T
NG_023284.1:g.70459G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_005807.6:c.3496C>T MANE Select	NP_005798.3:p.Arg1166Ter
ENST00000445192.7:c.3496C>T MANE Select	ENSP00000399679.3:p.Arg1166Ter
NM_001127708.2:c.3373C>T	NP_001121180.2:p.Arg1125Ter
NM_001127708.3:c.3373C>T	NP_001121180.2:p.Arg1125Ter
NM_001127709.2:c.3217C>T	NP_001121181.2:p.Arg1073Ter
NM_001127709.3:c.3217C>T	NP_001121181.2:p.Arg1073Ter
NM_001127710.2:c.3094C>T	NP_001121182.2:p.Arg1032Ter
NM_001127710.3:c.3094C>T	NP_001121182.2:p.Arg1032Ter
NM_001303232.1:c.3367C>T	NP_001290161.1:p.Arg1123Ter
NM_001303232.2:c.3367C>T	NP_001290161.1:p.Arg1123Ter
NM_005807.4:c.3496C>T	NP_005798.3:p.Arg1166Ter
ENST00000367483.8:c.3373C>T	ENSP00000356453.4:p.Arg1125Ter
ENST00000367485.4:c.3217C>T	ENSP00000356455.4:p.Arg1073Ter
ENST00000445192.6:c.3496C>T	ENSP00000399679.2:p.Arg1166Ter
ENST00000635041.1:c.3367C>T	ENSP00000489292.1:p.Arg1123Ter
XM_024448707.1:c.3496C>T	XP_024304475.1:p.Arg1166Ter
XM_024448717.1:c.3373C>T	XP_024304485.1:p.Arg1125Ter