Canonical Allele Identifier: CA2188861739

Gene: PSTPIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.77033048_77033051delinsCCTA , CM000677.2:g.77033048_77033051delinsCCTA	GRCh38
NC_000015.9:g.77325389_77325392delinsCCTA , CM000677.1:g.77325389_77325392delinsCCTA	GRCh37
NC_000015.8:g.75112444_75112447delinsCCTA	NCBI36
NG_007526.1:g.42925_42928delinsCCTA , LRG_172:g.42925_42928delinsCCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697622.1:n.2095+96_2095+99delinsCCTA
ENST00000697623.1:n.2348+96_2348+99delinsCCTA
ENST00000558012.6:c.929+96_929+99delinsCCTA MANE Select	ENSP00000452746.1:n.929+96_929+99delinsCCTA
ENST00000379595.7:c.929+96_929+99delinsCCTA	ENSP00000368914.3:n.929+96_929+99delinsCCTA
ENST00000557995.1:n.593+96_593+99delinsCCTA
ENST00000558012.5:c.929+96_929+99delinsCCTA	ENSP00000452746.1:n.929+96_929+99delinsCCTA
ENST00000558870.1:c.78+654_78+657delinsCCTA
ENST00000559295.5:c.872+620_872+623delinsCCTA	ENSP00000452743.1:n.872+620_872+623delinsCCTA
ENST00000559785.5:c.1158+96_1158+99delinsCCTA	ENSP00000452986.1:n.1158+96_1158+99delinsCCTA
ENST00000560223.5:c.*1031+96_*1031+99delinsCCTA	ENSP00000454118.1:n.*1031+96_*1031+99delinsCCTA
NM_003978.3:c.929+96_929+99delinsCCTA , LRG_172t1:c.929+96_929+99delinsCCTA	NP_003969.2:n.929+96_929+99delinsCCTA
XM_006720737.2:c.563+96_563+99delinsCCTA	XP_006720800.1:n.563+96_563+99delinsCCTA
XM_011522163.1:c.986+96_986+99delinsCCTA	XP_011520465.1:n.986+96_986+99delinsCCTA
XM_011522164.1:c.884+96_884+99delinsCCTA	XP_011520466.1:n.884+96_884+99delinsCCTA
XM_011522165.1:c.782+96_782+99delinsCCTA	XP_011520467.1:n.782+96_782+99delinsCCTA
XM_011522166.1:c.1020+96_1020+99delinsCCTA	XP_011520468.1:n.1020+96_1020+99delinsCCTA
XM_011522167.1:c.895+654_895+657delinsCCTA	XP_011520469.1:n.895+654_895+657delinsCCTA
XM_011522168.1:c.986+96_986+99delinsCCTA	XP_011520470.1:n.986+96_986+99delinsCCTA
XM_011522169.1:c.798+1770_798+1773delinsCCTA	XP_011520471.1:n.798+1770_798+1773delinsCCTA
XM_011522170.1:c.372-2460_372-2457delinsCCTA	XP_011520472.1:n.372-2460_372-2457delinsCCTA
XM_011522171.1:c.312-2460_312-2457delinsCCTA	XP_011520473.1:n.312-2460_312-2457delinsCCTA
XM_011522172.1:c.312-2460_312-2457delinsCCTA	XP_011520474.1:n.312-2460_312-2457delinsCCTA
XM_011522173.1:c.312-2460_312-2457delinsCCTA	XP_011520475.1:n.312-2460_312-2457delinsCCTA
XR_931936.1:n.1470+96_1470+99delinsCCTA
XR_931937.1:n.1413+96_1413+99delinsCCTA
XR_931938.1:n.1345+654_1345+657delinsCCTA
XR_931939.1:n.1248+1770_1248+1773delinsCCTA
XR_931940.1:n.1070-2460_1070-2457delinsCCTA
NM_001321135.1:c.872+620_872+623delinsCCTA	NP_001308064.1:n.872+620_872+623delinsCCTA
NM_001321136.1:c.902+96_902+99delinsCCTA	NP_001308065.1:n.902+96_902+99delinsCCTA
NM_001321137.1:c.1124+96_1124+99delinsCCTA	NP_001308066.1:n.1124+96_1124+99delinsCCTA
NM_003978.4:c.929+96_929+99delinsCCTA	NP_003969.2:n.929+96_929+99delinsCCTA
NR_135552.1:n.1150+1770_1150+1773delinsCCTA
XM_006720737.3:c.563+96_563+99delinsCCTA	XP_006720800.1:n.563+96_563+99delinsCCTA
XM_011522163.2:c.986+96_986+99delinsCCTA	XP_011520465.1:n.986+96_986+99delinsCCTA
XM_011522165.2:c.782+96_782+99delinsCCTA	XP_011520467.1:n.782+96_782+99delinsCCTA
XM_011522166.2:c.1020+96_1020+99delinsCCTA	XP_011520468.1:n.1020+96_1020+99delinsCCTA
XM_011522167.2:c.895+654_895+657delinsCCTA	XP_011520469.1:n.895+654_895+657delinsCCTA
XM_011522168.3:c.986+96_986+99delinsCCTA	XP_011520470.1:n.986+96_986+99delinsCCTA
XM_011522169.2:c.798+1770_798+1773delinsCCTA	XP_011520471.1:n.798+1770_798+1773delinsCCTA
XR_931936.2:n.1468+96_1468+99delinsCCTA
XR_931937.2:n.1411+96_1411+99delinsCCTA
XR_931938.2:n.1343+654_1343+657delinsCCTA
XR_931939.2:n.1246+1770_1246+1773delinsCCTA
NM_001321135.2:c.872+620_872+623delinsCCTA	NP_001308064.1:n.872+620_872+623delinsCCTA
NM_001321136.2:c.902+96_902+99delinsCCTA	NP_001308065.1:n.902+96_902+99delinsCCTA
NM_003978.5:c.929+96_929+99delinsCCTA MANE Select	NP_003969.2:n.929+96_929+99delinsCCTA
NR_135552.2:n.1109+1770_1109+1773delinsCCTA