Canonical Allele Identifier: CA1296572

Gene: PRG4

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186308973_186308979del , CM000663.2:g.186308973_186308979del	GRCh38
NC_000001.10:g.186278105_186278111del , CM000663.1:g.186278105_186278111del	GRCh37
NC_000001.9:g.184544728_184544734del	NCBI36
NG_008248.2:g.17688_17694del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445192.7:c.3254_3260del MANE Select	ENSP00000399679.3:p.Ser1085Ter
ENST00000367483.8:c.3131_3137del	ENSP00000356453.4:p.Ser1044Ter
ENST00000367485.4:c.2975_2981del	ENSP00000356455.4:p.Ser992Ter
ENST00000445192.6:c.3254_3260del	ENSP00000399679.2:p.Ser1085Ter
ENST00000635041.1:c.3125_3131del	ENSP00000489292.1:p.Ser1042Ter
NM_001127708.2:c.3131_3137del	NP_001121180.2:p.Ser1044Ter
NM_001127709.2:c.2975_2981del	NP_001121181.2:p.Ser992Ter
NM_001127710.2:c.2852_2858del	NP_001121182.2:p.Ser951Ter
NM_001303232.1:c.3125_3131del	NP_001290161.1:p.Ser1042Ter
NM_005807.4:c.3254_3260del	NP_005798.3:p.Ser1085Ter
XM_024448707.1:c.3254_3260del	XP_024304475.1:p.Ser1085Ter
XM_024448717.1:c.3131_3137del	XP_024304485.1:p.Ser1044Ter
NM_001127708.3:c.3131_3137del	NP_001121180.2:p.Ser1044Ter
NM_001127709.3:c.2975_2981del	NP_001121181.2:p.Ser992Ter
NM_001127710.3:c.2852_2858del	NP_001121182.2:p.Ser951Ter
NM_001303232.2:c.3125_3131del	NP_001290161.1:p.Ser1042Ter
NM_005807.6:c.3254_3260del MANE Select	NP_005798.3:p.Ser1085Ter