Canonical Allele Identifier: CA2188861352
Gene: PSTPIP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.77032363C= , CM000677.2:g.77032363C= GRCh38
NC_000015.9:g.77324704C= , CM000677.1:g.77324704C= GRCh37
NC_000015.8:g.75111759C= NCBI36
NG_007526.1:g.42240C= , LRG_172:g.42240C=

Transcript Alleles

HGVS Amino-acid change
ENST00000697622.1:n.1506C=
ENST00000697623.1:n.2226C=
ENST00000558012.6:c.807C= MANE Select ENSP00000452746.1:p.Ile269=
ENST00000379595.7:c.807C= ENSP00000368914.3:p.Ile269=
ENST00000557995.1:n.471C=
ENST00000558012.5:c.807C= ENSP00000452746.1:p.Ile269=
ENST00000558870.1:c.47C=
ENST00000559295.5:c.807C= ENSP00000452743.1:p.Ile269=
ENST00000559785.5:c.1002C= ENSP00000452986.1:p.Ile334=
ENST00000559856.1:c.726C= ENSP00000453382.1:p.Ile242=
ENST00000560223.5:c.*909C= ENSP00000454118.1:n.*909C=
ENST00000560377.5:n.1048C=
NM_003978.3:c.807C= , LRG_172t1:c.807C= NP_003969.2:p.Ile269=
XM_006720737.2:c.441C= XP_006720800.1:p.Ile147=
XM_011522163.1:c.864C= XP_011520465.1:p.Ile288=
XM_011522164.1:c.762C= XP_011520466.1:p.Ile254=
XM_011522165.1:c.660C= XP_011520467.1:p.Ile220=
XM_011522166.1:c.864C= XP_011520468.1:p.Ile288=
XM_011522167.1:c.864C= XP_011520469.1:p.Ile288=
XM_011522168.1:c.864C= XP_011520470.1:p.Ile288=
XM_011522169.1:c.798+1085C= XP_011520471.1:n.798+1085C=
XM_011522170.1:c.371+2789C= XP_011520472.1:n.371+2789C=
XM_011522171.1:c.311+2789C= XP_011520473.1:n.311+2789C=
XM_011522172.1:c.311+2789C= XP_011520474.1:n.311+2789C=
XM_011522173.1:c.311+2789C= XP_011520475.1:n.311+2789C=
XR_931936.1:n.1314C=
XR_931937.1:n.1257C=
XR_931938.1:n.1314C=
XR_931939.1:n.1248+1085C=
XR_931940.1:n.1069+2789C=
NM_001321135.1:c.807C= NP_001308064.1:p.Ile269=
NM_001321136.1:c.780C= NP_001308065.1:p.Ile260=
NM_001321137.1:c.1002C= NP_001308066.1:p.Ile334=
NM_003978.4:c.807C= NP_003969.2:p.Ile269=
NR_135552.1:n.1150+1085C=
XM_006720737.3:c.441C= XP_006720800.1:p.Ile147=
XM_011522163.2:c.864C= XP_011520465.1:p.Ile288=
XM_011522165.2:c.660C= XP_011520467.1:p.Ile220=
XM_011522166.2:c.864C= XP_011520468.1:p.Ile288=
XM_011522167.2:c.864C= XP_011520469.1:p.Ile288=
XM_011522168.3:c.864C= XP_011520470.1:p.Ile288=
XM_011522169.2:c.798+1085C= XP_011520471.1:n.798+1085C=
XR_931936.2:n.1312C=
XR_931937.2:n.1255C=
XR_931938.2:n.1312C=
XR_931939.2:n.1246+1085C=
NM_001321135.2:c.807C= NP_001308064.1:p.Ile269=
NM_001321136.2:c.780C= NP_001308065.1:p.Ile260=
NM_003978.5:c.807C= MANE Select NP_003969.2:p.Ile269=
NR_135552.2:n.1109+1085C=