Canonical Allele Identifier: CA971682666

Gene: PSTPIP1

Linked Data

• dbSNP Id: rs2076464625

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.77033156_77033157insG , CM000677.2:g.77033156_77033157insG	GRCh38
NC_000015.9:g.77325497_77325498insG , CM000677.1:g.77325497_77325498insG	GRCh37
NC_000015.8:g.75112552_75112553insG	NCBI36
NG_007526.1:g.43033_43034insG , LRG_172:g.43033_43034insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697622.1:n.2095+204_2095+205insG
ENST00000697623.1:n.2348+204_2348+205insG
ENST00000558012.6:c.929+204_929+205insG MANE Select	ENSP00000452746.1:n.929+204_929+205insG
ENST00000379595.7:c.929+204_929+205insG	ENSP00000368914.3:n.929+204_929+205insG
ENST00000557995.1:n.593+204_593+205insG
ENST00000558012.5:c.929+204_929+205insG	ENSP00000452746.1:n.929+204_929+205insG
ENST00000558870.1:c.78+762_78+763insG
ENST00000559295.5:c.872+728_872+729insG	ENSP00000452743.1:n.872+728_872+729insG
ENST00000559785.5:c.1158+204_1158+205insG	ENSP00000452986.1:n.1158+204_1158+205insG
ENST00000560223.5:c.*1031+204_*1031+205insG	ENSP00000454118.1:n.*1031+204_*1031+205insG
NM_003978.3:c.929+204_929+205insG , LRG_172t1:c.929+204_929+205insG	NP_003969.2:n.929+204_929+205insG
XM_006720737.2:c.563+204_563+205insG	XP_006720800.1:n.563+204_563+205insG
XM_011522163.1:c.986+204_986+205insG	XP_011520465.1:n.986+204_986+205insG
XM_011522164.1:c.884+204_884+205insG	XP_011520466.1:n.884+204_884+205insG
XM_011522165.1:c.782+204_782+205insG	XP_011520467.1:n.782+204_782+205insG
XM_011522166.1:c.1020+204_1020+205insG	XP_011520468.1:n.1020+204_1020+205insG
XM_011522167.1:c.895+762_895+763insG	XP_011520469.1:n.895+762_895+763insG
XM_011522168.1:c.986+204_986+205insG	XP_011520470.1:n.986+204_986+205insG
XM_011522169.1:c.798+1878_798+1879insG	XP_011520471.1:n.798+1878_798+1879insG
XM_011522170.1:c.372-2352_372-2351insG	XP_011520472.1:n.372-2352_372-2351insG
XM_011522171.1:c.312-2352_312-2351insG	XP_011520473.1:n.312-2352_312-2351insG
XM_011522172.1:c.312-2352_312-2351insG	XP_011520474.1:n.312-2352_312-2351insG
XM_011522173.1:c.312-2352_312-2351insG	XP_011520475.1:n.312-2352_312-2351insG
XR_931936.1:n.1470+204_1470+205insG
XR_931937.1:n.1413+204_1413+205insG
XR_931938.1:n.1345+762_1345+763insG
XR_931939.1:n.1248+1878_1248+1879insG
XR_931940.1:n.1070-2352_1070-2351insG
NM_001321135.1:c.872+728_872+729insG	NP_001308064.1:n.872+728_872+729insG
NM_001321136.1:c.902+204_902+205insG	NP_001308065.1:n.902+204_902+205insG
NM_001321137.1:c.1124+204_1124+205insG	NP_001308066.1:n.1124+204_1124+205insG
NM_003978.4:c.929+204_929+205insG	NP_003969.2:n.929+204_929+205insG
NR_135552.1:n.1150+1878_1150+1879insG
XM_006720737.3:c.563+204_563+205insG	XP_006720800.1:n.563+204_563+205insG
XM_011522163.2:c.986+204_986+205insG	XP_011520465.1:n.986+204_986+205insG
XM_011522165.2:c.782+204_782+205insG	XP_011520467.1:n.782+204_782+205insG
XM_011522166.2:c.1020+204_1020+205insG	XP_011520468.1:n.1020+204_1020+205insG
XM_011522167.2:c.895+762_895+763insG	XP_011520469.1:n.895+762_895+763insG
XM_011522168.3:c.986+204_986+205insG	XP_011520470.1:n.986+204_986+205insG
XM_011522169.2:c.798+1878_798+1879insG	XP_011520471.1:n.798+1878_798+1879insG
XR_931936.2:n.1468+204_1468+205insG
XR_931937.2:n.1411+204_1411+205insG
XR_931938.2:n.1343+762_1343+763insG
XR_931939.2:n.1246+1878_1246+1879insG
NM_001321135.2:c.872+728_872+729insG	NP_001308064.1:n.872+728_872+729insG
NM_001321136.2:c.902+204_902+205insG	NP_001308065.1:n.902+204_902+205insG
NM_003978.5:c.929+204_929+205insG MANE Select	NP_003969.2:n.929+204_929+205insG
NR_135552.2:n.1109+1878_1109+1879insG