Canonical Allele Identifier: CA2188861658

Gene: PSTPIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.77032893G= , CM000677.2:g.77032893G=	GRCh38
NC_000015.9:g.77325234G= , CM000677.1:g.77325234G=	GRCh37
NC_000015.8:g.75112289G=	NCBI36
NG_007526.1:g.42770G= , LRG_172:g.42770G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697622.1:n.2036G=
ENST00000697623.1:n.2289G=
ENST00000558012.6:c.870G= MANE Select	ENSP00000452746.1:p.Arg290=
ENST00000379595.7:c.870G=	ENSP00000368914.3:p.Arg290=
ENST00000557995.1:n.534G=
ENST00000558012.5:c.870G=	ENSP00000452746.1:p.Arg290=
ENST00000558870.1:c.78+499G=
ENST00000559295.5:c.872+465G=	ENSP00000452743.1:n.872+465G=
ENST00000559785.5:c.1099G=	ENSP00000452986.1:p.Gly367=
ENST00000560223.5:c.*972G=	ENSP00000454118.1:n.*972G=
NM_003978.3:c.870G= , LRG_172t1:c.870G=	NP_003969.2:p.Arg290=
XM_006720737.2:c.504G=	XP_006720800.1:p.Arg168=
XM_011522163.1:c.927G=	XP_011520465.1:p.Arg309=
XM_011522164.1:c.825G=	XP_011520466.1:p.Arg275=
XM_011522165.1:c.723G=	XP_011520467.1:p.Arg241=
XM_011522166.1:c.961G=	XP_011520468.1:p.Gly321=
XM_011522167.1:c.895+499G=	XP_011520469.1:n.895+499G=
XM_011522168.1:c.927G=	XP_011520470.1:p.Arg309=
XM_011522169.1:c.798+1615G=	XP_011520471.1:n.798+1615G=
XM_011522170.1:c.372-2615G=	XP_011520472.1:n.372-2615G=
XM_011522171.1:c.312-2615G=	XP_011520473.1:n.312-2615G=
XM_011522172.1:c.312-2615G=	XP_011520474.1:n.312-2615G=
XM_011522173.1:c.312-2615G=	XP_011520475.1:n.312-2615G=
XR_931936.1:n.1411G=
XR_931937.1:n.1354G=
XR_931938.1:n.1345+499G=
XR_931939.1:n.1248+1615G=
XR_931940.1:n.1070-2615G=
NM_001321135.1:c.872+465G=	NP_001308064.1:n.872+465G=
NM_001321136.1:c.843G=	NP_001308065.1:p.Arg281=
NM_001321137.1:c.1065G=	NP_001308066.1:p.Arg355=
NM_003978.4:c.870G=	NP_003969.2:p.Arg290=
NR_135552.1:n.1150+1615G=
XM_006720737.3:c.504G=	XP_006720800.1:p.Arg168=
XM_011522163.2:c.927G=	XP_011520465.1:p.Arg309=
XM_011522165.2:c.723G=	XP_011520467.1:p.Arg241=
XM_011522166.2:c.961G=	XP_011520468.1:p.Gly321=
XM_011522167.2:c.895+499G=	XP_011520469.1:n.895+499G=
XM_011522168.3:c.927G=	XP_011520470.1:p.Arg309=
XM_011522169.2:c.798+1615G=	XP_011520471.1:n.798+1615G=
XR_931936.2:n.1409G=
XR_931937.2:n.1352G=
XR_931938.2:n.1343+499G=
XR_931939.2:n.1246+1615G=
NM_001321135.2:c.872+465G=	NP_001308064.1:n.872+465G=
NM_001321136.2:c.843G=	NP_001308065.1:p.Arg281=
NM_003978.5:c.870G= MANE Select	NP_003969.2:p.Arg290=
NR_135552.2:n.1109+1615G=