Canonical Allele Identifier: CA2188861540
Gene: PSTPIP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.77032710C= , CM000677.2:g.77032710C= GRCh38
NC_000015.9:g.77325051C= , CM000677.1:g.77325051C= GRCh37
NC_000015.8:g.75112106C= NCBI36
NG_007526.1:g.42587C= , LRG_172:g.42587C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000697622.1:n.1853C=
ENST00000697623.1:n.2258-152C=
ENST00000558012.6:c.839-152C= MANE Select ENSP00000452746.1:n.839-152C=
ENST00000379595.7:c.839-152C= ENSP00000368914.3:n.839-152C=
ENST00000557995.1:n.503-152C=
ENST00000558012.5:c.839-152C= ENSP00000452746.1:n.839-152C=
ENST00000558870.1:c.78+316C=
ENST00000559295.5:c.872+282C= ENSP00000452743.1:n.872+282C=
ENST00000559785.5:c.1068-152C= ENSP00000452986.1:n.1068-152C=
ENST00000560223.5:c.*941-152C= ENSP00000454118.1:n.*941-152C=
ENST00000560377.5:n.1395C=
NM_003978.3:c.839-152C= , LRG_172t1:c.839-152C= NP_003969.2:n.839-152C=
XM_006720737.2:c.473-152C= XP_006720800.1:n.473-152C=
XM_011522163.1:c.896-152C= XP_011520465.1:n.896-152C=
XM_011522164.1:c.794-152C= XP_011520466.1:n.794-152C=
XM_011522165.1:c.692-152C= XP_011520467.1:n.692-152C=
XM_011522166.1:c.930-152C= XP_011520468.1:n.930-152C=
XM_011522167.1:c.895+316C= XP_011520469.1:n.895+316C=
XM_011522168.1:c.896-152C= XP_011520470.1:n.896-152C=
XM_011522169.1:c.798+1432C= XP_011520471.1:n.798+1432C=
XM_011522170.1:c.372-2798C= XP_011520472.1:n.372-2798C=
XM_011522171.1:c.312-2798C= XP_011520473.1:n.312-2798C=
XM_011522172.1:c.312-2798C= XP_011520474.1:n.312-2798C=
XM_011522173.1:c.312-2798C= XP_011520475.1:n.312-2798C=
XR_931936.1:n.1380-152C=
XR_931937.1:n.1323-152C=
XR_931938.1:n.1345+316C=
XR_931939.1:n.1248+1432C=
XR_931940.1:n.1070-2798C=
NM_001321135.1:c.872+282C= NP_001308064.1:n.872+282C=
NM_001321136.1:c.812-152C= NP_001308065.1:n.812-152C=
NM_001321137.1:c.1034-152C= NP_001308066.1:n.1034-152C=
NM_003978.4:c.839-152C= NP_003969.2:n.839-152C=
NR_135552.1:n.1150+1432C=
XM_006720737.3:c.473-152C= XP_006720800.1:n.473-152C=
XM_011522163.2:c.896-152C= XP_011520465.1:n.896-152C=
XM_011522165.2:c.692-152C= XP_011520467.1:n.692-152C=
XM_011522166.2:c.930-152C= XP_011520468.1:n.930-152C=
XM_011522167.2:c.895+316C= XP_011520469.1:n.895+316C=
XM_011522168.3:c.896-152C= XP_011520470.1:n.896-152C=
XM_011522169.2:c.798+1432C= XP_011520471.1:n.798+1432C=
XR_931936.2:n.1378-152C=
XR_931937.2:n.1321-152C=
XR_931938.2:n.1343+316C=
XR_931939.2:n.1246+1432C=
NM_001321135.2:c.872+282C= NP_001308064.1:n.872+282C=
NM_001321136.2:c.812-152C= NP_001308065.1:n.812-152C=
NM_003978.5:c.839-152C= MANE Select NP_003969.2:n.839-152C=
NR_135552.2:n.1109+1432C=