Canonical Allele Identifier: CA491336001

Gene: PSTPIP1

Linked Data

• gnomAD v4: 15-77032902-C-T
• MyVariant Identifiers: chr15:g.77325243C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.77032902C>T , CM000677.2:g.77032902C>T	GRCh38
NC_000015.9:g.77325243C>T , CM000677.1:g.77325243C>T	GRCh37
NC_000015.8:g.75112298C>T	NCBI36
NG_007526.1:g.42779C>T , LRG_172:g.42779C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697622.1:n.2045C>T
ENST00000697623.1:n.2298C>T
ENST00000558012.6:c.879C>T MANE Select	ENSP00000452746.1:p.Thr293=
ENST00000379595.7:c.879C>T	ENSP00000368914.3:p.Thr293=
ENST00000557995.1:n.543C>T
ENST00000558012.5:c.879C>T	ENSP00000452746.1:p.Thr293=
ENST00000558870.1:c.78+508C>T
ENST00000559295.5:c.872+474C>T	ENSP00000452743.1:n.872+474C>T
ENST00000559785.5:c.1108C>T	ENSP00000452986.1:p.Pro370Ser
ENST00000560223.5:c.*981C>T	ENSP00000454118.1:n.*981C>T
NM_003978.3:c.879C>T , LRG_172t1:c.879C>T	NP_003969.2:p.Thr293=
XM_006720737.2:c.513C>T	XP_006720800.1:p.Thr171=
XM_011522163.1:c.936C>T	XP_011520465.1:p.Thr312=
XM_011522164.1:c.834C>T	XP_011520466.1:p.Thr278=
XM_011522165.1:c.732C>T	XP_011520467.1:p.Thr244=
XM_011522166.1:c.970C>T	XP_011520468.1:p.Pro324Ser
XM_011522167.1:c.895+508C>T	XP_011520469.1:n.895+508C>T
XM_011522168.1:c.936C>T	XP_011520470.1:p.Thr312=
XM_011522169.1:c.798+1624C>T	XP_011520471.1:n.798+1624C>T
XM_011522170.1:c.372-2606C>T	XP_011520472.1:n.372-2606C>T
XM_011522171.1:c.312-2606C>T	XP_011520473.1:n.312-2606C>T
XM_011522172.1:c.312-2606C>T	XP_011520474.1:n.312-2606C>T
XM_011522173.1:c.312-2606C>T	XP_011520475.1:n.312-2606C>T
XR_931936.1:n.1420C>T
XR_931937.1:n.1363C>T
XR_931938.1:n.1345+508C>T
XR_931939.1:n.1248+1624C>T
XR_931940.1:n.1070-2606C>T
NM_001321135.1:c.872+474C>T	NP_001308064.1:n.872+474C>T
NM_001321136.1:c.852C>T	NP_001308065.1:p.Thr284=
NM_001321137.1:c.1074C>T	NP_001308066.1:p.Thr358=
NM_003978.4:c.879C>T	NP_003969.2:p.Thr293=
NR_135552.1:n.1150+1624C>T
XM_006720737.3:c.513C>T	XP_006720800.1:p.Thr171=
XM_011522163.2:c.936C>T	XP_011520465.1:p.Thr312=
XM_011522165.2:c.732C>T	XP_011520467.1:p.Thr244=
XM_011522166.2:c.970C>T	XP_011520468.1:p.Pro324Ser
XM_011522167.2:c.895+508C>T	XP_011520469.1:n.895+508C>T
XM_011522168.3:c.936C>T	XP_011520470.1:p.Thr312=
XM_011522169.2:c.798+1624C>T	XP_011520471.1:n.798+1624C>T
XR_931936.2:n.1418C>T
XR_931937.2:n.1361C>T
XR_931938.2:n.1343+508C>T
XR_931939.2:n.1246+1624C>T
NM_001321135.2:c.872+474C>T	NP_001308064.1:n.872+474C>T
NM_001321136.2:c.852C>T	NP_001308065.1:p.Thr284=
NM_003978.5:c.879C>T MANE Select	NP_003969.2:p.Thr293=
NR_135552.2:n.1109+1624C>T