Canonical Allele Identifier: CA2188861323

Gene: PSTPIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.77032314G= , CM000677.2:g.77032314G=	GRCh38
NC_000015.9:g.77324655G= , CM000677.1:g.77324655G=	GRCh37
NC_000015.8:g.75111710G=	NCBI36
NG_007526.1:g.42191G= , LRG_172:g.42191G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697622.1:n.1457G=
ENST00000697623.1:n.2177G=
ENST00000558012.6:c.758G= MANE Select	ENSP00000452746.1:p.Arg253=
ENST00000379595.7:c.758G=	ENSP00000368914.3:p.Arg253=
ENST00000557995.1:n.422G=
ENST00000558012.5:c.758G=	ENSP00000452746.1:p.Arg253=
ENST00000559295.5:c.758G=	ENSP00000452743.1:p.Arg253=
ENST00000559785.5:c.953G=	ENSP00000452986.1:p.Arg318=
ENST00000559856.1:c.677G=	ENSP00000453382.1:p.Arg226=
ENST00000560223.5:c.*860G=	ENSP00000454118.1:n.*860G=
ENST00000560377.5:n.999G=
NM_003978.3:c.758G= , LRG_172t1:c.758G=	NP_003969.2:p.Arg253=
XM_006720737.2:c.392G=	XP_006720800.1:p.Arg131=
XM_011522163.1:c.815G=	XP_011520465.1:p.Arg272=
XM_011522164.1:c.713G=	XP_011520466.1:p.Arg238=
XM_011522165.1:c.611G=	XP_011520467.1:p.Arg204=
XM_011522166.1:c.815G=	XP_011520468.1:p.Arg272=
XM_011522167.1:c.815G=	XP_011520469.1:p.Arg272=
XM_011522168.1:c.815G=	XP_011520470.1:p.Arg272=
XM_011522169.1:c.798+1036G=	XP_011520471.1:n.798+1036G=
XM_011522170.1:c.371+2740G=	XP_011520472.1:n.371+2740G=
XM_011522171.1:c.311+2740G=	XP_011520473.1:n.311+2740G=
XM_011522172.1:c.311+2740G=	XP_011520474.1:n.311+2740G=
XM_011522173.1:c.311+2740G=	XP_011520475.1:n.311+2740G=
XR_931936.1:n.1265G=
XR_931937.1:n.1208G=
XR_931938.1:n.1265G=
XR_931939.1:n.1248+1036G=
XR_931940.1:n.1069+2740G=
NM_001321135.1:c.758G=	NP_001308064.1:p.Arg253=
NM_001321136.1:c.731G=	NP_001308065.1:p.Arg244=
NM_001321137.1:c.953G=	NP_001308066.1:p.Arg318=
NM_003978.4:c.758G=	NP_003969.2:p.Arg253=
NR_135552.1:n.1150+1036G=
XM_006720737.3:c.392G=	XP_006720800.1:p.Arg131=
XM_011522163.2:c.815G=	XP_011520465.1:p.Arg272=
XM_011522165.2:c.611G=	XP_011520467.1:p.Arg204=
XM_011522166.2:c.815G=	XP_011520468.1:p.Arg272=
XM_011522167.2:c.815G=	XP_011520469.1:p.Arg272=
XM_011522168.3:c.815G=	XP_011520470.1:p.Arg272=
XM_011522169.2:c.798+1036G=	XP_011520471.1:n.798+1036G=
XR_931936.2:n.1263G=
XR_931937.2:n.1206G=
XR_931938.2:n.1263G=
XR_931939.2:n.1246+1036G=
NM_001321135.2:c.758G=	NP_001308064.1:p.Arg253=
NM_001321136.2:c.731G=	NP_001308065.1:p.Arg244=
NM_003978.5:c.758G= MANE Select	NP_003969.2:p.Arg253=
NR_135552.2:n.1109+1036G=