Canonical Allele Identifier: CA2188861682

Gene: PSTPIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.77032935C= , CM000677.2:g.77032935C=	GRCh38
NC_000015.9:g.77325276C= , CM000677.1:g.77325276C=	GRCh37
NC_000015.8:g.75112331C=	NCBI36
NG_007526.1:g.42812C= , LRG_172:g.42812C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000697622.1:n.2078C=
ENST00000697623.1:n.2331C=
ENST00000558012.6:c.912C= MANE Select	ENSP00000452746.1:p.Ser304=
ENST00000379595.7:c.912C=	ENSP00000368914.3:p.Ser304=
ENST00000557995.1:n.576C=
ENST00000558012.5:c.912C=	ENSP00000452746.1:p.Ser304=
ENST00000558870.1:c.78+541C=
ENST00000559295.5:c.872+507C=	ENSP00000452743.1:n.872+507C=
ENST00000559785.5:c.1141C=	ENSP00000452986.1:p.Leu381=
ENST00000560223.5:c.*1014C=	ENSP00000454118.1:n.*1014C=
NM_003978.3:c.912C= , LRG_172t1:c.912C=	NP_003969.2:p.Ser304=
XM_006720737.2:c.546C=	XP_006720800.1:p.Ser182=
XM_011522163.1:c.969C=	XP_011520465.1:p.Ser323=
XM_011522164.1:c.867C=	XP_011520466.1:p.Ser289=
XM_011522165.1:c.765C=	XP_011520467.1:p.Ser255=
XM_011522166.1:c.1003C=	XP_011520468.1:p.Leu335=
XM_011522167.1:c.895+541C=	XP_011520469.1:n.895+541C=
XM_011522168.1:c.969C=	XP_011520470.1:p.Ser323=
XM_011522169.1:c.798+1657C=	XP_011520471.1:n.798+1657C=
XM_011522170.1:c.372-2573C=	XP_011520472.1:n.372-2573C=
XM_011522171.1:c.312-2573C=	XP_011520473.1:n.312-2573C=
XM_011522172.1:c.312-2573C=	XP_011520474.1:n.312-2573C=
XM_011522173.1:c.312-2573C=	XP_011520475.1:n.312-2573C=
XR_931936.1:n.1453C=
XR_931937.1:n.1396C=
XR_931938.1:n.1345+541C=
XR_931939.1:n.1248+1657C=
XR_931940.1:n.1070-2573C=
NM_001321135.1:c.872+507C=	NP_001308064.1:n.872+507C=
NM_001321136.1:c.885C=	NP_001308065.1:p.Ser295=
NM_001321137.1:c.1107C=	NP_001308066.1:p.Ser369=
NM_003978.4:c.912C=	NP_003969.2:p.Ser304=
NR_135552.1:n.1150+1657C=
XM_006720737.3:c.546C=	XP_006720800.1:p.Ser182=
XM_011522163.2:c.969C=	XP_011520465.1:p.Ser323=
XM_011522165.2:c.765C=	XP_011520467.1:p.Ser255=
XM_011522166.2:c.1003C=	XP_011520468.1:p.Leu335=
XM_011522167.2:c.895+541C=	XP_011520469.1:n.895+541C=
XM_011522168.3:c.969C=	XP_011520470.1:p.Ser323=
XM_011522169.2:c.798+1657C=	XP_011520471.1:n.798+1657C=
XR_931936.2:n.1451C=
XR_931937.2:n.1394C=
XR_931938.2:n.1343+541C=
XR_931939.2:n.1246+1657C=
NM_001321135.2:c.872+507C=	NP_001308064.1:n.872+507C=
NM_001321136.2:c.885C=	NP_001308065.1:p.Ser295=
NM_003978.5:c.912C= MANE Select	NP_003969.2:p.Ser304=
NR_135552.2:n.1109+1657C=