Canonical Allele Identifier: CA2804830615

Gene: PSTPIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.77033100_77033101insATT , CM000677.2:g.77033100_77033101insATT	GRCh38
NC_000015.9:g.77325441_77325442insATT , CM000677.1:g.77325441_77325442insATT	GRCh37
NC_000015.8:g.75112496_75112497insATT	NCBI36
NG_007526.1:g.42977_42978insATT , LRG_172:g.42977_42978insATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697622.1:n.2095+148_2095+149insATT
ENST00000697623.1:n.2348+148_2348+149insATT
ENST00000558012.6:c.929+148_929+149insATT MANE Select	ENSP00000452746.1:n.929+148_929+149insATT
ENST00000379595.7:c.929+148_929+149insATT	ENSP00000368914.3:n.929+148_929+149insATT
ENST00000557995.1:n.593+148_593+149insATT
ENST00000558012.5:c.929+148_929+149insATT	ENSP00000452746.1:n.929+148_929+149insATT
ENST00000558870.1:c.78+706_78+707insATT
ENST00000559295.5:c.872+672_872+673insATT	ENSP00000452743.1:n.872+672_872+673insATT
ENST00000559785.5:c.1158+148_1158+149insATT	ENSP00000452986.1:n.1158+148_1158+149insATT
ENST00000560223.5:c.*1031+148_*1031+149insATT	ENSP00000454118.1:n.*1031+148_*1031+149insATT
NM_003978.3:c.929+148_929+149insATT , LRG_172t1:c.929+148_929+149insATT	NP_003969.2:n.929+148_929+149insATT
XM_006720737.2:c.563+148_563+149insATT	XP_006720800.1:n.563+148_563+149insATT
XM_011522163.1:c.986+148_986+149insATT	XP_011520465.1:n.986+148_986+149insATT
XM_011522164.1:c.884+148_884+149insATT	XP_011520466.1:n.884+148_884+149insATT
XM_011522165.1:c.782+148_782+149insATT	XP_011520467.1:n.782+148_782+149insATT
XM_011522166.1:c.1020+148_1020+149insATT	XP_011520468.1:n.1020+148_1020+149insATT
XM_011522167.1:c.895+706_895+707insATT	XP_011520469.1:n.895+706_895+707insATT
XM_011522168.1:c.986+148_986+149insATT	XP_011520470.1:n.986+148_986+149insATT
XM_011522169.1:c.798+1822_798+1823insATT	XP_011520471.1:n.798+1822_798+1823insATT
XM_011522170.1:c.372-2408_372-2407insATT	XP_011520472.1:n.372-2408_372-2407insATT
XM_011522171.1:c.312-2408_312-2407insATT	XP_011520473.1:n.312-2408_312-2407insATT
XM_011522172.1:c.312-2408_312-2407insATT	XP_011520474.1:n.312-2408_312-2407insATT
XM_011522173.1:c.312-2408_312-2407insATT	XP_011520475.1:n.312-2408_312-2407insATT
XR_931936.1:n.1470+148_1470+149insATT
XR_931937.1:n.1413+148_1413+149insATT
XR_931938.1:n.1345+706_1345+707insATT
XR_931939.1:n.1248+1822_1248+1823insATT
XR_931940.1:n.1070-2408_1070-2407insATT
NM_001321135.1:c.872+672_872+673insATT	NP_001308064.1:n.872+672_872+673insATT
NM_001321136.1:c.902+148_902+149insATT	NP_001308065.1:n.902+148_902+149insATT
NM_001321137.1:c.1124+148_1124+149insATT	NP_001308066.1:n.1124+148_1124+149insATT
NM_003978.4:c.929+148_929+149insATT	NP_003969.2:n.929+148_929+149insATT
NR_135552.1:n.1150+1822_1150+1823insATT
XM_006720737.3:c.563+148_563+149insATT	XP_006720800.1:n.563+148_563+149insATT
XM_011522163.2:c.986+148_986+149insATT	XP_011520465.1:n.986+148_986+149insATT
XM_011522165.2:c.782+148_782+149insATT	XP_011520467.1:n.782+148_782+149insATT
XM_011522166.2:c.1020+148_1020+149insATT	XP_011520468.1:n.1020+148_1020+149insATT
XM_011522167.2:c.895+706_895+707insATT	XP_011520469.1:n.895+706_895+707insATT
XM_011522168.3:c.986+148_986+149insATT	XP_011520470.1:n.986+148_986+149insATT
XM_011522169.2:c.798+1822_798+1823insATT	XP_011520471.1:n.798+1822_798+1823insATT
XR_931936.2:n.1468+148_1468+149insATT
XR_931937.2:n.1411+148_1411+149insATT
XR_931938.2:n.1343+706_1343+707insATT
XR_931939.2:n.1246+1822_1246+1823insATT
NM_001321135.2:c.872+672_872+673insATT	NP_001308064.1:n.872+672_872+673insATT
NM_001321136.2:c.902+148_902+149insATT	NP_001308065.1:n.902+148_902+149insATT
NM_003978.5:c.929+148_929+149insATT MANE Select	NP_003969.2:n.929+148_929+149insATT
NR_135552.2:n.1109+1822_1109+1823insATT