Canonical Allele Identifier: CA2575798915

Gene: PSTPIP1

Linked Data

• gnomAD v4: 15-77032217-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.77032222del , CM000677.2:g.77032222del	GRCh38
NC_000015.9:g.77324563del , CM000677.1:g.77324563del	GRCh37
NC_000015.8:g.75111618del	NCBI36
NG_007526.1:g.42099del , LRG_172:g.42099del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697622.1:n.1365del
ENST00000697623.1:n.2085del
ENST00000558012.6:c.742-76del MANE Select	ENSP00000452746.1:n.742-76del
ENST00000379595.7:c.742-76del	ENSP00000368914.3:n.742-76del
ENST00000557995.1:n.406-76del
ENST00000558012.5:c.742-76del	ENSP00000452746.1:n.742-76del
ENST00000559295.5:c.742-76del	ENSP00000452743.1:n.742-76del
ENST00000559785.5:c.937-76del	ENSP00000452986.1:n.937-76del
ENST00000559856.1:c.661-76del	ENSP00000453382.1:n.661-76del
ENST00000560223.5:c.*844-76del	ENSP00000454118.1:n.*844-76del
ENST00000560377.5:n.983-76del
NM_003978.3:c.742-76del , LRG_172t1:c.742-76del	NP_003969.2:n.742-76del
XM_006720737.2:c.376-76del	XP_006720800.1:n.376-76del
XM_011522163.1:c.799-76del	XP_011520465.1:n.799-76del
XM_011522164.1:c.697-76del	XP_011520466.1:n.697-76del
XM_011522165.1:c.595-76del	XP_011520467.1:n.595-76del
XM_011522166.1:c.799-76del	XP_011520468.1:n.799-76del
XM_011522167.1:c.799-76del	XP_011520469.1:n.799-76del
XM_011522168.1:c.799-76del	XP_011520470.1:n.799-76del
XM_011522169.1:c.798+944del	XP_011520471.1:n.798+944del
XM_011522170.1:c.371+2648del	XP_011520472.1:n.371+2648del
XM_011522171.1:c.311+2648del	XP_011520473.1:n.311+2648del
XM_011522172.1:c.311+2648del	XP_011520474.1:n.311+2648del
XM_011522173.1:c.311+2648del	XP_011520475.1:n.311+2648del
XR_931936.1:n.1249-76del
XR_931937.1:n.1192-76del
XR_931938.1:n.1249-76del
XR_931939.1:n.1248+944del
XR_931940.1:n.1069+2648del
NM_001321135.1:c.742-76del	NP_001308064.1:n.742-76del
NM_001321136.1:c.715-76del	NP_001308065.1:n.715-76del
NM_001321137.1:c.937-76del	NP_001308066.1:n.937-76del
NM_003978.4:c.742-76del	NP_003969.2:n.742-76del
NR_135552.1:n.1150+944del
XM_006720737.3:c.376-76del	XP_006720800.1:n.376-76del
XM_011522163.2:c.799-76del	XP_011520465.1:n.799-76del
XM_011522165.2:c.595-76del	XP_011520467.1:n.595-76del
XM_011522166.2:c.799-76del	XP_011520468.1:n.799-76del
XM_011522167.2:c.799-76del	XP_011520469.1:n.799-76del
XM_011522168.3:c.799-76del	XP_011520470.1:n.799-76del
XM_011522169.2:c.798+944del	XP_011520471.1:n.798+944del
XR_931936.2:n.1247-76del
XR_931937.2:n.1190-76del
XR_931938.2:n.1247-76del
XR_931939.2:n.1246+944del
NM_001321135.2:c.742-76del	NP_001308064.1:n.742-76del
NM_001321136.2:c.715-76del	NP_001308065.1:n.715-76del
NM_003978.5:c.742-76del MANE Select	NP_003969.2:n.742-76del
NR_135552.2:n.1109+944del