Canonical Allele Identifier: CA491336032

Gene: PSTPIP1

Linked Data

• MyVariant Identifiers: chr15:g.77325292A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.77032951A>C , CM000677.2:g.77032951A>C	GRCh38
NC_000015.9:g.77325292A>C , CM000677.1:g.77325292A>C	GRCh37
NC_000015.8:g.75112347A>C	NCBI36
NG_007526.1:g.42828A>C , LRG_172:g.42828A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697622.1:n.2094A>C
ENST00000697623.1:n.2347A>C
ENST00000558012.6:c.928A>C MANE Select	ENSP00000452746.1:p.Arg310=
ENST00000379595.7:c.928A>C	ENSP00000368914.3:p.Arg310=
ENST00000557995.1:n.592A>C
ENST00000558012.5:c.928A>C	ENSP00000452746.1:p.Arg310=
ENST00000558870.1:c.78+557A>C
ENST00000559295.5:c.872+523A>C	ENSP00000452743.1:n.872+523A>C
ENST00000559785.5:c.1157A>C	ENSP00000452986.1:p.Glu386Ala
ENST00000560223.5:c.*1030A>C	ENSP00000454118.1:n.*1030A>C
NM_003978.3:c.928A>C , LRG_172t1:c.928A>C	NP_003969.2:p.Arg310=
XM_006720737.2:c.562A>C	XP_006720800.1:p.Arg188=
XM_011522163.1:c.985A>C	XP_011520465.1:p.Arg329=
XM_011522164.1:c.883A>C	XP_011520466.1:p.Arg295=
XM_011522165.1:c.781A>C	XP_011520467.1:p.Arg261=
XM_011522166.1:c.1019A>C	XP_011520468.1:p.Glu340Ala
XM_011522167.1:c.895+557A>C	XP_011520469.1:n.895+557A>C
XM_011522168.1:c.985A>C	XP_011520470.1:p.Arg329=
XM_011522169.1:c.798+1673A>C	XP_011520471.1:n.798+1673A>C
XM_011522170.1:c.372-2557A>C	XP_011520472.1:n.372-2557A>C
XM_011522171.1:c.312-2557A>C	XP_011520473.1:n.312-2557A>C
XM_011522172.1:c.312-2557A>C	XP_011520474.1:n.312-2557A>C
XM_011522173.1:c.312-2557A>C	XP_011520475.1:n.312-2557A>C
XR_931936.1:n.1469A>C
XR_931937.1:n.1412A>C
XR_931938.1:n.1345+557A>C
XR_931939.1:n.1248+1673A>C
XR_931940.1:n.1070-2557A>C
NM_001321135.1:c.872+523A>C	NP_001308064.1:n.872+523A>C
NM_001321136.1:c.901A>C	NP_001308065.1:p.Arg301=
NM_001321137.1:c.1123A>C	NP_001308066.1:p.Arg375=
NM_003978.4:c.928A>C	NP_003969.2:p.Arg310=
NR_135552.1:n.1150+1673A>C
XM_006720737.3:c.562A>C	XP_006720800.1:p.Arg188=
XM_011522163.2:c.985A>C	XP_011520465.1:p.Arg329=
XM_011522165.2:c.781A>C	XP_011520467.1:p.Arg261=
XM_011522166.2:c.1019A>C	XP_011520468.1:p.Glu340Ala
XM_011522167.2:c.895+557A>C	XP_011520469.1:n.895+557A>C
XM_011522168.3:c.985A>C	XP_011520470.1:p.Arg329=
XM_011522169.2:c.798+1673A>C	XP_011520471.1:n.798+1673A>C
XR_931936.2:n.1467A>C
XR_931937.2:n.1410A>C
XR_931938.2:n.1343+557A>C
XR_931939.2:n.1246+1673A>C
NM_001321135.2:c.872+523A>C	NP_001308064.1:n.872+523A>C
NM_001321136.2:c.901A>C	NP_001308065.1:p.Arg301=
NM_003978.5:c.928A>C MANE Select	NP_003969.2:p.Arg310=
NR_135552.2:n.1109+1673A>C