Canonical Allele Identifier: CA919594687
Gene: PSTPIP1 HGNC NCBI

Linked Data

dbSNP Id: rs1568521280

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.77032597dup , CM000677.2:g.77032597dup GRCh38
NC_000015.9:g.77324938dup , CM000677.1:g.77324938dup GRCh37
NC_000015.8:g.75111993dup NCBI36
NG_007526.1:g.42474dup , LRG_172:g.42474dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000697622.1:n.1740dup
ENST00000697623.1:n.2257+203dup
ENST00000558012.6:c.838+203dup MANE Select ENSP00000452746.1:n.838+203dup
ENST00000379595.7:c.838+203dup ENSP00000368914.3:n.838+203dup
ENST00000557995.1:n.502+203dup
ENST00000558012.5:c.838+203dup ENSP00000452746.1:n.838+203dup
ENST00000558870.1:c.78+203dup
ENST00000559295.5:c.872+169dup ENSP00000452743.1:n.872+169dup
ENST00000559785.5:c.1067+169dup ENSP00000452986.1:n.1067+169dup
ENST00000560223.5:c.*940+203dup ENSP00000454118.1:n.*940+203dup
ENST00000560377.5:n.1282dup
NM_003978.3:c.838+203dup , LRG_172t1:c.838+203dup NP_003969.2:n.838+203dup
XM_006720737.2:c.472+203dup XP_006720800.1:n.472+203dup
XM_011522163.1:c.895+203dup XP_011520465.1:n.895+203dup
XM_011522164.1:c.793+203dup XP_011520466.1:n.793+203dup
XM_011522165.1:c.691+203dup XP_011520467.1:n.691+203dup
XM_011522166.1:c.929+169dup XP_011520468.1:n.929+169dup
XM_011522167.1:c.895+203dup XP_011520469.1:n.895+203dup
XM_011522168.1:c.895+203dup XP_011520470.1:n.895+203dup
XM_011522169.1:c.798+1319dup XP_011520471.1:n.798+1319dup
XM_011522170.1:c.372-2911dup XP_011520472.1:n.372-2911dup
XM_011522171.1:c.312-2911dup XP_011520473.1:n.312-2911dup
XM_011522172.1:c.312-2911dup XP_011520474.1:n.312-2911dup
XM_011522173.1:c.312-2911dup XP_011520475.1:n.312-2911dup
XR_931936.1:n.1379+169dup
XR_931937.1:n.1322+169dup
XR_931938.1:n.1345+203dup
XR_931939.1:n.1248+1319dup
XR_931940.1:n.1070-2911dup
NM_001321135.1:c.872+169dup NP_001308064.1:n.872+169dup
NM_001321136.1:c.811+203dup NP_001308065.1:n.811+203dup
NM_001321137.1:c.1033+203dup NP_001308066.1:n.1033+203dup
NM_003978.4:c.838+203dup NP_003969.2:n.838+203dup
NR_135552.1:n.1150+1319dup
XM_006720737.3:c.472+203dup XP_006720800.1:n.472+203dup
XM_011522163.2:c.895+203dup XP_011520465.1:n.895+203dup
XM_011522165.2:c.691+203dup XP_011520467.1:n.691+203dup
XM_011522166.2:c.929+169dup XP_011520468.1:n.929+169dup
XM_011522167.2:c.895+203dup XP_011520469.1:n.895+203dup
XM_011522168.3:c.895+203dup XP_011520470.1:n.895+203dup
XM_011522169.2:c.798+1319dup XP_011520471.1:n.798+1319dup
XR_931936.2:n.1377+169dup
XR_931937.2:n.1320+169dup
XR_931938.2:n.1343+203dup
XR_931939.2:n.1246+1319dup
NM_001321135.2:c.872+169dup NP_001308064.1:n.872+169dup
NM_001321136.2:c.811+203dup NP_001308065.1:n.811+203dup
NM_003978.5:c.838+203dup MANE Select NP_003969.2:n.838+203dup
NR_135552.2:n.1109+1319dup