Canonical Allele Identifier: CA273760792

Gene: PSTPIP1

Linked Data

• ClinVar Variation Id: 2789195
• ClinVar RCV Id: RCV003611847
• dbSNP Id: rs753081335
• gnomAD v3: 15-77032963-G-C
• gnomAD v4: 15-77032963-G-C
• MyVariant Identifiers: chr15:g.77325304G>C (hg19) ; chr15:g.77032963G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.77032963G>C , CM000677.2:g.77032963G>C	GRCh38
NC_000015.9:g.77325304G>C , CM000677.1:g.77325304G>C	GRCh37
NC_000015.8:g.75112359G>C	NCBI36
NG_007526.1:g.42840G>C , LRG_172:g.42840G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697622.1:n.2095+11G>C
ENST00000697623.1:n.2348+11G>C
ENST00000558012.6:c.929+11G>C MANE Select	ENSP00000452746.1:n.929+11G>C
ENST00000379595.7:c.929+11G>C	ENSP00000368914.3:n.929+11G>C
ENST00000557995.1:n.593+11G>C
ENST00000558012.5:c.929+11G>C	ENSP00000452746.1:n.929+11G>C
ENST00000558870.1:c.78+569G>C
ENST00000559295.5:c.872+535G>C	ENSP00000452743.1:n.872+535G>C
ENST00000559785.5:c.1158+11G>C	ENSP00000452986.1:n.1158+11G>C
ENST00000560223.5:c.*1031+11G>C	ENSP00000454118.1:n.*1031+11G>C
NM_003978.3:c.929+11G>C , LRG_172t1:c.929+11G>C	NP_003969.2:n.929+11G>C
XM_006720737.2:c.563+11G>C	XP_006720800.1:n.563+11G>C
XM_011522163.1:c.986+11G>C	XP_011520465.1:n.986+11G>C
XM_011522164.1:c.884+11G>C	XP_011520466.1:n.884+11G>C
XM_011522165.1:c.782+11G>C	XP_011520467.1:n.782+11G>C
XM_011522166.1:c.1020+11G>C	XP_011520468.1:n.1020+11G>C
XM_011522167.1:c.895+569G>C	XP_011520469.1:n.895+569G>C
XM_011522168.1:c.986+11G>C	XP_011520470.1:n.986+11G>C
XM_011522169.1:c.798+1685G>C	XP_011520471.1:n.798+1685G>C
XM_011522170.1:c.372-2545G>C	XP_011520472.1:n.372-2545G>C
XM_011522171.1:c.312-2545G>C	XP_011520473.1:n.312-2545G>C
XM_011522172.1:c.312-2545G>C	XP_011520474.1:n.312-2545G>C
XM_011522173.1:c.312-2545G>C	XP_011520475.1:n.312-2545G>C
XR_931936.1:n.1470+11G>C
XR_931937.1:n.1413+11G>C
XR_931938.1:n.1345+569G>C
XR_931939.1:n.1248+1685G>C
XR_931940.1:n.1070-2545G>C
NM_001321135.1:c.872+535G>C	NP_001308064.1:n.872+535G>C
NM_001321136.1:c.902+11G>C	NP_001308065.1:n.902+11G>C
NM_001321137.1:c.1124+11G>C	NP_001308066.1:n.1124+11G>C
NM_003978.4:c.929+11G>C	NP_003969.2:n.929+11G>C
NR_135552.1:n.1150+1685G>C
XM_006720737.3:c.563+11G>C	XP_006720800.1:n.563+11G>C
XM_011522163.2:c.986+11G>C	XP_011520465.1:n.986+11G>C
XM_011522165.2:c.782+11G>C	XP_011520467.1:n.782+11G>C
XM_011522166.2:c.1020+11G>C	XP_011520468.1:n.1020+11G>C
XM_011522167.2:c.895+569G>C	XP_011520469.1:n.895+569G>C
XM_011522168.3:c.986+11G>C	XP_011520470.1:n.986+11G>C
XM_011522169.2:c.798+1685G>C	XP_011520471.1:n.798+1685G>C
XR_931936.2:n.1468+11G>C
XR_931937.2:n.1411+11G>C
XR_931938.2:n.1343+569G>C
XR_931939.2:n.1246+1685G>C
NM_001321135.2:c.872+535G>C	NP_001308064.1:n.872+535G>C
NM_001321136.2:c.902+11G>C	NP_001308065.1:n.902+11G>C
NM_003978.5:c.929+11G>C MANE Select	NP_003969.2:n.929+11G>C
NR_135552.2:n.1109+1685G>C