Canonical Allele Identifier: CA393520795

Gene: PSTPIP1

Linked Data

• MyVariant Identifiers: chr15:g.77322922G>T (hg19) ; chr15:g.77030581G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.77030581G>T , CM000677.2:g.77030581G>T	GRCh38
NC_000015.9:g.77322922G>T , CM000677.1:g.77322922G>T	GRCh37
NC_000015.8:g.75109977G>T	NCBI36
NG_007526.1:g.40458G>T , LRG_172:g.40458G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000697622.1:n.322G>T
ENST00000697623.1:n.1042G>T
ENST00000558012.6:c.642G>T MANE Select	ENSP00000452746.1:p.Glu214Asp
ENST00000379595.7:c.642G>T	ENSP00000368914.3:p.Glu214Asp
ENST00000557995.1:n.306G>T
ENST00000558012.5:c.642G>T	ENSP00000452746.1:p.Glu214Asp
ENST00000559295.5:c.642G>T	ENSP00000452743.1:p.Glu214Asp
ENST00000559750.5:c.*283G>T	ENSP00000453531.1:n.*283G>T
ENST00000559785.5:c.837G>T	ENSP00000452986.1:p.Glu279Asp
ENST00000559856.1:c.561G>T	ENSP00000453382.1:p.Glu187Asp
ENST00000560223.5:c.*744G>T	ENSP00000454118.1:n.*744G>T
ENST00000560377.5:n.883G>T
ENST00000561315.5:n.415G>T
NM_003978.3:c.642G>T , LRG_172t1:c.642G>T	NP_003969.2:p.Glu214Asp
XM_006720737.2:c.276G>T	XP_006720800.1:p.Glu92Asp
XM_011522163.1:c.699G>T	XP_011520465.1:p.Glu233Asp
XM_011522164.1:c.597G>T	XP_011520466.1:p.Glu199Asp
XM_011522165.1:c.495G>T	XP_011520467.1:p.Glu165Asp
XM_011522166.1:c.699G>T	XP_011520468.1:p.Glu233Asp
XM_011522167.1:c.699G>T	XP_011520469.1:p.Glu233Asp
XM_011522168.1:c.699G>T	XP_011520470.1:p.Glu233Asp
XM_011522169.1:c.699G>T	XP_011520471.1:p.Glu233Asp
XM_011522170.1:c.371+1007G>T	XP_011520472.1:n.371+1007G>T
XM_011522171.1:c.311+1007G>T	XP_011520473.1:n.311+1007G>T
XM_011522172.1:c.311+1007G>T	XP_011520474.1:n.311+1007G>T
XM_011522173.1:c.311+1007G>T	XP_011520475.1:n.311+1007G>T
XR_931936.1:n.1149G>T
XR_931937.1:n.1092G>T
XR_931938.1:n.1149G>T
XR_931939.1:n.1149G>T
XR_931940.1:n.1069+1007G>T
NM_001321135.1:c.642G>T	NP_001308064.1:p.Glu214Asp
NM_001321136.1:c.615G>T	NP_001308065.1:p.Glu205Asp
NM_001321137.1:c.837G>T	NP_001308066.1:p.Glu279Asp
NM_003978.4:c.642G>T	NP_003969.2:p.Glu214Asp
NR_135552.1:n.1052-599G>T
XM_006720737.3:c.276G>T	XP_006720800.1:p.Glu92Asp
XM_011522163.2:c.699G>T	XP_011520465.1:p.Glu233Asp
XM_011522165.2:c.495G>T	XP_011520467.1:p.Glu165Asp
XM_011522166.2:c.699G>T	XP_011520468.1:p.Glu233Asp
XM_011522167.2:c.699G>T	XP_011520469.1:p.Glu233Asp
XM_011522168.3:c.699G>T	XP_011520470.1:p.Glu233Asp
XM_011522169.2:c.699G>T	XP_011520471.1:p.Glu233Asp
XR_931936.2:n.1147G>T
XR_931937.2:n.1090G>T
XR_931938.2:n.1147G>T
XR_931939.2:n.1147G>T
NM_001321135.2:c.642G>T	NP_001308064.1:p.Glu214Asp
NM_001321136.2:c.615G>T	NP_001308065.1:p.Glu205Asp
NM_003978.5:c.642G>T MANE Select	NP_003969.2:p.Glu214Asp
NR_135552.2:n.1011-599G>T