Canonical Allele Identifier: CA491336027

Gene: PSTPIP1

Linked Data

• MyVariant Identifiers: chr15:g.77325282C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.77032941C>G , CM000677.2:g.77032941C>G	GRCh38
NC_000015.9:g.77325282C>G , CM000677.1:g.77325282C>G	GRCh37
NC_000015.8:g.75112337C>G	NCBI36
NG_007526.1:g.42818C>G , LRG_172:g.42818C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000697622.1:n.2084C>G
ENST00000697623.1:n.2337C>G
ENST00000558012.6:c.918C>G MANE Select	ENSP00000452746.1:p.Gly306=
ENST00000379595.7:c.918C>G	ENSP00000368914.3:p.Gly306=
ENST00000557995.1:n.582C>G
ENST00000558012.5:c.918C>G	ENSP00000452746.1:p.Gly306=
ENST00000558870.1:c.78+547C>G
ENST00000559295.5:c.872+513C>G	ENSP00000452743.1:n.872+513C>G
ENST00000559785.5:c.1147C>G	ENSP00000452986.1:p.His383Asp
ENST00000560223.5:c.*1020C>G	ENSP00000454118.1:n.*1020C>G
NM_003978.3:c.918C>G , LRG_172t1:c.918C>G	NP_003969.2:p.Gly306=
XM_006720737.2:c.552C>G	XP_006720800.1:p.Gly184=
XM_011522163.1:c.975C>G	XP_011520465.1:p.Gly325=
XM_011522164.1:c.873C>G	XP_011520466.1:p.Gly291=
XM_011522165.1:c.771C>G	XP_011520467.1:p.Gly257=
XM_011522166.1:c.1009C>G	XP_011520468.1:p.His337Asp
XM_011522167.1:c.895+547C>G	XP_011520469.1:n.895+547C>G
XM_011522168.1:c.975C>G	XP_011520470.1:p.Gly325=
XM_011522169.1:c.798+1663C>G	XP_011520471.1:n.798+1663C>G
XM_011522170.1:c.372-2567C>G	XP_011520472.1:n.372-2567C>G
XM_011522171.1:c.312-2567C>G	XP_011520473.1:n.312-2567C>G
XM_011522172.1:c.312-2567C>G	XP_011520474.1:n.312-2567C>G
XM_011522173.1:c.312-2567C>G	XP_011520475.1:n.312-2567C>G
XR_931936.1:n.1459C>G
XR_931937.1:n.1402C>G
XR_931938.1:n.1345+547C>G
XR_931939.1:n.1248+1663C>G
XR_931940.1:n.1070-2567C>G
NM_001321135.1:c.872+513C>G	NP_001308064.1:n.872+513C>G
NM_001321136.1:c.891C>G	NP_001308065.1:p.Gly297=
NM_001321137.1:c.1113C>G	NP_001308066.1:p.Gly371=
NM_003978.4:c.918C>G	NP_003969.2:p.Gly306=
NR_135552.1:n.1150+1663C>G
XM_006720737.3:c.552C>G	XP_006720800.1:p.Gly184=
XM_011522163.2:c.975C>G	XP_011520465.1:p.Gly325=
XM_011522165.2:c.771C>G	XP_011520467.1:p.Gly257=
XM_011522166.2:c.1009C>G	XP_011520468.1:p.His337Asp
XM_011522167.2:c.895+547C>G	XP_011520469.1:n.895+547C>G
XM_011522168.3:c.975C>G	XP_011520470.1:p.Gly325=
XM_011522169.2:c.798+1663C>G	XP_011520471.1:n.798+1663C>G
XR_931936.2:n.1457C>G
XR_931937.2:n.1400C>G
XR_931938.2:n.1343+547C>G
XR_931939.2:n.1246+1663C>G
NM_001321135.2:c.872+513C>G	NP_001308064.1:n.872+513C>G
NM_001321136.2:c.891C>G	NP_001308065.1:p.Gly297=
NM_003978.5:c.918C>G MANE Select	NP_003969.2:p.Gly306=
NR_135552.2:n.1109+1663C>G