Canonical Allele Identifier: CA2188861474
Gene: PSTPIP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.77032569A= , CM000677.2:g.77032569A= GRCh38
NC_000015.9:g.77324910A= , CM000677.1:g.77324910A= GRCh37
NC_000015.8:g.75111965A= NCBI36
NG_007526.1:g.42446A= , LRG_172:g.42446A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000697622.1:n.1712A=
ENST00000697623.1:n.2257+175A=
ENST00000558012.6:c.838+175A= MANE Select ENSP00000452746.1:n.838+175A=
ENST00000379595.7:c.838+175A= ENSP00000368914.3:n.838+175A=
ENST00000557995.1:n.502+175A=
ENST00000558012.5:c.838+175A= ENSP00000452746.1:n.838+175A=
ENST00000558870.1:c.78+175A=
ENST00000559295.5:c.872+141A= ENSP00000452743.1:n.872+141A=
ENST00000559785.5:c.1067+141A= ENSP00000452986.1:n.1067+141A=
ENST00000560223.5:c.*940+175A= ENSP00000454118.1:n.*940+175A=
ENST00000560377.5:n.1254A=
NM_003978.3:c.838+175A= , LRG_172t1:c.838+175A= NP_003969.2:n.838+175A=
XM_006720737.2:c.472+175A= XP_006720800.1:n.472+175A=
XM_011522163.1:c.895+175A= XP_011520465.1:n.895+175A=
XM_011522164.1:c.793+175A= XP_011520466.1:n.793+175A=
XM_011522165.1:c.691+175A= XP_011520467.1:n.691+175A=
XM_011522166.1:c.929+141A= XP_011520468.1:n.929+141A=
XM_011522167.1:c.895+175A= XP_011520469.1:n.895+175A=
XM_011522168.1:c.895+175A= XP_011520470.1:n.895+175A=
XM_011522169.1:c.798+1291A= XP_011520471.1:n.798+1291A=
XM_011522170.1:c.372-2939A= XP_011520472.1:n.372-2939A=
XM_011522171.1:c.312-2939A= XP_011520473.1:n.312-2939A=
XM_011522172.1:c.312-2939A= XP_011520474.1:n.312-2939A=
XM_011522173.1:c.312-2939A= XP_011520475.1:n.312-2939A=
XR_931936.1:n.1379+141A=
XR_931937.1:n.1322+141A=
XR_931938.1:n.1345+175A=
XR_931939.1:n.1248+1291A=
XR_931940.1:n.1070-2939A=
NM_001321135.1:c.872+141A= NP_001308064.1:n.872+141A=
NM_001321136.1:c.811+175A= NP_001308065.1:n.811+175A=
NM_001321137.1:c.1033+175A= NP_001308066.1:n.1033+175A=
NM_003978.4:c.838+175A= NP_003969.2:n.838+175A=
NR_135552.1:n.1150+1291A=
XM_006720737.3:c.472+175A= XP_006720800.1:n.472+175A=
XM_011522163.2:c.895+175A= XP_011520465.1:n.895+175A=
XM_011522165.2:c.691+175A= XP_011520467.1:n.691+175A=
XM_011522166.2:c.929+141A= XP_011520468.1:n.929+141A=
XM_011522167.2:c.895+175A= XP_011520469.1:n.895+175A=
XM_011522168.3:c.895+175A= XP_011520470.1:n.895+175A=
XM_011522169.2:c.798+1291A= XP_011520471.1:n.798+1291A=
XR_931936.2:n.1377+141A=
XR_931937.2:n.1320+141A=
XR_931938.2:n.1343+175A=
XR_931939.2:n.1246+1291A=
NM_001321135.2:c.872+141A= NP_001308064.1:n.872+141A=
NM_001321136.2:c.811+175A= NP_001308065.1:n.811+175A=
NM_003978.5:c.838+175A= MANE Select NP_003969.2:n.838+175A=
NR_135552.2:n.1109+1291A=