Canonical Allele Identifier: CA393521478

Gene: PSTPIP1

Linked Data

• MyVariant Identifiers: chr15:g.77325283A>G (hg19) ; chr15:g.77032942A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.77032942A>G , CM000677.2:g.77032942A>G	GRCh38
NC_000015.9:g.77325283A>G , CM000677.1:g.77325283A>G	GRCh37
NC_000015.8:g.75112338A>G	NCBI36
NG_007526.1:g.42819A>G , LRG_172:g.42819A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000697622.1:n.2085A>G
ENST00000697623.1:n.2338A>G
ENST00000558012.6:c.919A>G MANE Select	ENSP00000452746.1:p.Met307Val
ENST00000379595.7:c.919A>G	ENSP00000368914.3:p.Met307Val
ENST00000557995.1:n.583A>G
ENST00000558012.5:c.919A>G	ENSP00000452746.1:p.Met307Val
ENST00000558870.1:c.78+548A>G
ENST00000559295.5:c.872+514A>G	ENSP00000452743.1:n.872+514A>G
ENST00000559785.5:c.1148A>G	ENSP00000452986.1:p.His383Arg
ENST00000560223.5:c.*1021A>G	ENSP00000454118.1:n.*1021A>G
NM_003978.3:c.919A>G , LRG_172t1:c.919A>G	NP_003969.2:p.Met307Val
XM_006720737.2:c.553A>G	XP_006720800.1:p.Met185Val
XM_011522163.1:c.976A>G	XP_011520465.1:p.Met326Val
XM_011522164.1:c.874A>G	XP_011520466.1:p.Met292Val
XM_011522165.1:c.772A>G	XP_011520467.1:p.Met258Val
XM_011522166.1:c.1010A>G	XP_011520468.1:p.His337Arg
XM_011522167.1:c.895+548A>G	XP_011520469.1:n.895+548A>G
XM_011522168.1:c.976A>G	XP_011520470.1:p.Met326Val
XM_011522169.1:c.798+1664A>G	XP_011520471.1:n.798+1664A>G
XM_011522170.1:c.372-2566A>G	XP_011520472.1:n.372-2566A>G
XM_011522171.1:c.312-2566A>G	XP_011520473.1:n.312-2566A>G
XM_011522172.1:c.312-2566A>G	XP_011520474.1:n.312-2566A>G
XM_011522173.1:c.312-2566A>G	XP_011520475.1:n.312-2566A>G
XR_931936.1:n.1460A>G
XR_931937.1:n.1403A>G
XR_931938.1:n.1345+548A>G
XR_931939.1:n.1248+1664A>G
XR_931940.1:n.1070-2566A>G
NM_001321135.1:c.872+514A>G	NP_001308064.1:n.872+514A>G
NM_001321136.1:c.892A>G	NP_001308065.1:p.Met298Val
NM_001321137.1:c.1114A>G	NP_001308066.1:p.Met372Val
NM_003978.4:c.919A>G	NP_003969.2:p.Met307Val
NR_135552.1:n.1150+1664A>G
XM_006720737.3:c.553A>G	XP_006720800.1:p.Met185Val
XM_011522163.2:c.976A>G	XP_011520465.1:p.Met326Val
XM_011522165.2:c.772A>G	XP_011520467.1:p.Met258Val
XM_011522166.2:c.1010A>G	XP_011520468.1:p.His337Arg
XM_011522167.2:c.895+548A>G	XP_011520469.1:n.895+548A>G
XM_011522168.3:c.976A>G	XP_011520470.1:p.Met326Val
XM_011522169.2:c.798+1664A>G	XP_011520471.1:n.798+1664A>G
XR_931936.2:n.1458A>G
XR_931937.2:n.1401A>G
XR_931938.2:n.1343+548A>G
XR_931939.2:n.1246+1664A>G
NM_001321135.2:c.872+514A>G	NP_001308064.1:n.872+514A>G
NM_001321136.2:c.892A>G	NP_001308065.1:p.Met298Val
NM_003978.5:c.919A>G MANE Select	NP_003969.2:p.Met307Val
NR_135552.2:n.1109+1664A>G