Canonical Allele Identifier: CA2629651335
Gene: PSTPIP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.77032538del , CM000677.2:g.77032538del GRCh38
NC_000015.9:g.77324879del , CM000677.1:g.77324879del GRCh37
NC_000015.8:g.75111934del NCBI36
NG_007526.1:g.42415del , LRG_172:g.42415del

Transcript Alleles

HGVS Amino-acid Change
ENST00000697622.1:n.1681del
ENST00000697623.1:n.2257+144del
ENST00000558012.6:c.838+144del MANE Select ENSP00000452746.1:n.838+144del
ENST00000379595.7:c.838+144del ENSP00000368914.3:n.838+144del
ENST00000557995.1:n.502+144del
ENST00000558012.5:c.838+144del ENSP00000452746.1:n.838+144del
ENST00000558870.1:c.78+144del
ENST00000559295.5:c.872+110del ENSP00000452743.1:n.872+110del
ENST00000559785.5:c.1067+110del ENSP00000452986.1:n.1067+110del
ENST00000560223.5:c.*940+144del ENSP00000454118.1:n.*940+144del
ENST00000560377.5:n.1223del
NM_003978.3:c.838+144del , LRG_172t1:c.838+144del NP_003969.2:n.838+144del
XM_006720737.2:c.472+144del XP_006720800.1:n.472+144del
XM_011522163.1:c.895+144del XP_011520465.1:n.895+144del
XM_011522164.1:c.793+144del XP_011520466.1:n.793+144del
XM_011522165.1:c.691+144del XP_011520467.1:n.691+144del
XM_011522166.1:c.929+110del XP_011520468.1:n.929+110del
XM_011522167.1:c.895+144del XP_011520469.1:n.895+144del
XM_011522168.1:c.895+144del XP_011520470.1:n.895+144del
XM_011522169.1:c.798+1260del XP_011520471.1:n.798+1260del
XM_011522170.1:c.371+2964del XP_011520472.1:n.371+2964del
XM_011522171.1:c.311+2964del XP_011520473.1:n.311+2964del
XM_011522172.1:c.311+2964del XP_011520474.1:n.311+2964del
XM_011522173.1:c.311+2964del XP_011520475.1:n.311+2964del
XR_931936.1:n.1379+110del
XR_931937.1:n.1322+110del
XR_931938.1:n.1345+144del
XR_931939.1:n.1248+1260del
XR_931940.1:n.1069+2964del
NM_001321135.1:c.872+110del NP_001308064.1:n.872+110del
NM_001321136.1:c.811+144del NP_001308065.1:n.811+144del
NM_001321137.1:c.1033+144del NP_001308066.1:n.1033+144del
NM_003978.4:c.838+144del NP_003969.2:n.838+144del
NR_135552.1:n.1150+1260del
XM_006720737.3:c.472+144del XP_006720800.1:n.472+144del
XM_011522163.2:c.895+144del XP_011520465.1:n.895+144del
XM_011522165.2:c.691+144del XP_011520467.1:n.691+144del
XM_011522166.2:c.929+110del XP_011520468.1:n.929+110del
XM_011522167.2:c.895+144del XP_011520469.1:n.895+144del
XM_011522168.3:c.895+144del XP_011520470.1:n.895+144del
XM_011522169.2:c.798+1260del XP_011520471.1:n.798+1260del
XR_931936.2:n.1377+110del
XR_931937.2:n.1320+110del
XR_931938.2:n.1343+144del
XR_931939.2:n.1246+1260del
NM_001321135.2:c.872+110del NP_001308064.1:n.872+110del
NM_001321136.2:c.811+144del NP_001308065.1:n.811+144del
NM_003978.5:c.838+144del MANE Select NP_003969.2:n.838+144del
NR_135552.2:n.1109+1260del