Canonical Allele Identifier: CA619193379

Gene: PSTPIP1

Linked Data

• dbSNP Id: rs1481938655
• gnomAD v2: 15-77325468-G-A
• gnomAD v3: 15-77033127-G-A
• gnomAD v4: 15-77033127-G-A
• MyVariant Identifiers: chr15:g.77325468G>A (hg19) ; chr15:g.77033127G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.77033127G>A , CM000677.2:g.77033127G>A	GRCh38
NC_000015.9:g.77325468G>A , CM000677.1:g.77325468G>A	GRCh37
NC_000015.8:g.75112523G>A	NCBI36
NG_007526.1:g.43004G>A , LRG_172:g.43004G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697622.1:n.2095+175G>A
ENST00000697623.1:n.2348+175G>A
ENST00000558012.6:c.929+175G>A MANE Select	ENSP00000452746.1:n.929+175G>A
ENST00000379595.7:c.929+175G>A	ENSP00000368914.3:n.929+175G>A
ENST00000557995.1:n.593+175G>A
ENST00000558012.5:c.929+175G>A	ENSP00000452746.1:n.929+175G>A
ENST00000558870.1:c.78+733G>A
ENST00000559295.5:c.872+699G>A	ENSP00000452743.1:n.872+699G>A
ENST00000559785.5:c.1158+175G>A	ENSP00000452986.1:n.1158+175G>A
ENST00000560223.5:c.*1031+175G>A	ENSP00000454118.1:n.*1031+175G>A
NM_003978.3:c.929+175G>A , LRG_172t1:c.929+175G>A	NP_003969.2:n.929+175G>A
XM_006720737.2:c.563+175G>A	XP_006720800.1:n.563+175G>A
XM_011522163.1:c.986+175G>A	XP_011520465.1:n.986+175G>A
XM_011522164.1:c.884+175G>A	XP_011520466.1:n.884+175G>A
XM_011522165.1:c.782+175G>A	XP_011520467.1:n.782+175G>A
XM_011522166.1:c.1020+175G>A	XP_011520468.1:n.1020+175G>A
XM_011522167.1:c.895+733G>A	XP_011520469.1:n.895+733G>A
XM_011522168.1:c.986+175G>A	XP_011520470.1:n.986+175G>A
XM_011522169.1:c.798+1849G>A	XP_011520471.1:n.798+1849G>A
XM_011522170.1:c.372-2381G>A	XP_011520472.1:n.372-2381G>A
XM_011522171.1:c.312-2381G>A	XP_011520473.1:n.312-2381G>A
XM_011522172.1:c.312-2381G>A	XP_011520474.1:n.312-2381G>A
XM_011522173.1:c.312-2381G>A	XP_011520475.1:n.312-2381G>A
XR_931936.1:n.1470+175G>A
XR_931937.1:n.1413+175G>A
XR_931938.1:n.1345+733G>A
XR_931939.1:n.1248+1849G>A
XR_931940.1:n.1070-2381G>A
NM_001321135.1:c.872+699G>A	NP_001308064.1:n.872+699G>A
NM_001321136.1:c.902+175G>A	NP_001308065.1:n.902+175G>A
NM_001321137.1:c.1124+175G>A	NP_001308066.1:n.1124+175G>A
NM_003978.4:c.929+175G>A	NP_003969.2:n.929+175G>A
NR_135552.1:n.1150+1849G>A
XM_006720737.3:c.563+175G>A	XP_006720800.1:n.563+175G>A
XM_011522163.2:c.986+175G>A	XP_011520465.1:n.986+175G>A
XM_011522165.2:c.782+175G>A	XP_011520467.1:n.782+175G>A
XM_011522166.2:c.1020+175G>A	XP_011520468.1:n.1020+175G>A
XM_011522167.2:c.895+733G>A	XP_011520469.1:n.895+733G>A
XM_011522168.3:c.986+175G>A	XP_011520470.1:n.986+175G>A
XM_011522169.2:c.798+1849G>A	XP_011520471.1:n.798+1849G>A
XR_931936.2:n.1468+175G>A
XR_931937.2:n.1411+175G>A
XR_931938.2:n.1343+733G>A
XR_931939.2:n.1246+1849G>A
NM_001321135.2:c.872+699G>A	NP_001308064.1:n.872+699G>A
NM_001321136.2:c.902+175G>A	NP_001308065.1:n.902+175G>A
NM_003978.5:c.929+175G>A MANE Select	NP_003969.2:n.929+175G>A
NR_135552.2:n.1109+1849G>A