Canonical Allele Identifier: CA393521494

Gene: PSTPIP1

Linked Data

• MyVariant Identifiers: chr15:g.77325289A>T (hg19) ; chr15:g.77032948A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.77032948A>T , CM000677.2:g.77032948A>T	GRCh38
NC_000015.9:g.77325289A>T , CM000677.1:g.77325289A>T	GRCh37
NC_000015.8:g.75112344A>T	NCBI36
NG_007526.1:g.42825A>T , LRG_172:g.42825A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697622.1:n.2091A>T
ENST00000697623.1:n.2344A>T
ENST00000558012.6:c.925A>T MANE Select	ENSP00000452746.1:p.Lys309Ter
ENST00000379595.7:c.925A>T	ENSP00000368914.3:p.Lys309Ter
ENST00000557995.1:n.589A>T
ENST00000558012.5:c.925A>T	ENSP00000452746.1:p.Lys309Ter
ENST00000558870.1:c.78+554A>T
ENST00000559295.5:c.872+520A>T	ENSP00000452743.1:n.872+520A>T
ENST00000559785.5:c.1154A>T	ENSP00000452986.1:p.Lys385Ile
ENST00000560223.5:c.*1027A>T	ENSP00000454118.1:n.*1027A>T
NM_003978.3:c.925A>T , LRG_172t1:c.925A>T	NP_003969.2:p.Lys309Ter
XM_006720737.2:c.559A>T	XP_006720800.1:p.Lys187Ter
XM_011522163.1:c.982A>T	XP_011520465.1:p.Lys328Ter
XM_011522164.1:c.880A>T	XP_011520466.1:p.Lys294Ter
XM_011522165.1:c.778A>T	XP_011520467.1:p.Lys260Ter
XM_011522166.1:c.1016A>T	XP_011520468.1:p.Lys339Ile
XM_011522167.1:c.895+554A>T	XP_011520469.1:n.895+554A>T
XM_011522168.1:c.982A>T	XP_011520470.1:p.Lys328Ter
XM_011522169.1:c.798+1670A>T	XP_011520471.1:n.798+1670A>T
XM_011522170.1:c.372-2560A>T	XP_011520472.1:n.372-2560A>T
XM_011522171.1:c.312-2560A>T	XP_011520473.1:n.312-2560A>T
XM_011522172.1:c.312-2560A>T	XP_011520474.1:n.312-2560A>T
XM_011522173.1:c.312-2560A>T	XP_011520475.1:n.312-2560A>T
XR_931936.1:n.1466A>T
XR_931937.1:n.1409A>T
XR_931938.1:n.1345+554A>T
XR_931939.1:n.1248+1670A>T
XR_931940.1:n.1070-2560A>T
NM_001321135.1:c.872+520A>T	NP_001308064.1:n.872+520A>T
NM_001321136.1:c.898A>T	NP_001308065.1:p.Lys300Ter
NM_001321137.1:c.1120A>T	NP_001308066.1:p.Lys374Ter
NM_003978.4:c.925A>T	NP_003969.2:p.Lys309Ter
NR_135552.1:n.1150+1670A>T
XM_006720737.3:c.559A>T	XP_006720800.1:p.Lys187Ter
XM_011522163.2:c.982A>T	XP_011520465.1:p.Lys328Ter
XM_011522165.2:c.778A>T	XP_011520467.1:p.Lys260Ter
XM_011522166.2:c.1016A>T	XP_011520468.1:p.Lys339Ile
XM_011522167.2:c.895+554A>T	XP_011520469.1:n.895+554A>T
XM_011522168.3:c.982A>T	XP_011520470.1:p.Lys328Ter
XM_011522169.2:c.798+1670A>T	XP_011520471.1:n.798+1670A>T
XR_931936.2:n.1464A>T
XR_931937.2:n.1407A>T
XR_931938.2:n.1343+554A>T
XR_931939.2:n.1246+1670A>T
NM_001321135.2:c.872+520A>T	NP_001308064.1:n.872+520A>T
NM_001321136.2:c.898A>T	NP_001308065.1:p.Lys300Ter
NM_003978.5:c.925A>T MANE Select	NP_003969.2:p.Lys309Ter
NR_135552.2:n.1109+1670A>T