Canonical Allele Identifier: CA393521414

Gene: PSTPIP1

Linked Data

• MyVariant Identifiers: chr15:g.77325251C>G (hg19) ; chr15:g.77032910C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.77032910C>G , CM000677.2:g.77032910C>G	GRCh38
NC_000015.9:g.77325251C>G , CM000677.1:g.77325251C>G	GRCh37
NC_000015.8:g.75112306C>G	NCBI36
NG_007526.1:g.42787C>G , LRG_172:g.42787C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697622.1:n.2053C>G
ENST00000697623.1:n.2306C>G
ENST00000558012.6:c.887C>G MANE Select	ENSP00000452746.1:p.Thr296Ser
ENST00000379595.7:c.887C>G	ENSP00000368914.3:p.Thr296Ser
ENST00000557995.1:n.551C>G
ENST00000558012.5:c.887C>G	ENSP00000452746.1:p.Thr296Ser
ENST00000558870.1:c.78+516C>G
ENST00000559295.5:c.872+482C>G	ENSP00000452743.1:n.872+482C>G
ENST00000559785.5:c.1116C>G	ENSP00000452986.1:p.Asp372Glu
ENST00000560223.5:c.*989C>G	ENSP00000454118.1:n.*989C>G
NM_003978.3:c.887C>G , LRG_172t1:c.887C>G	NP_003969.2:p.Thr296Ser
XM_006720737.2:c.521C>G	XP_006720800.1:p.Thr174Ser
XM_011522163.1:c.944C>G	XP_011520465.1:p.Thr315Ser
XM_011522164.1:c.842C>G	XP_011520466.1:p.Thr281Ser
XM_011522165.1:c.740C>G	XP_011520467.1:p.Thr247Ser
XM_011522166.1:c.978C>G	XP_011520468.1:p.Asp326Glu
XM_011522167.1:c.895+516C>G	XP_011520469.1:n.895+516C>G
XM_011522168.1:c.944C>G	XP_011520470.1:p.Thr315Ser
XM_011522169.1:c.798+1632C>G	XP_011520471.1:n.798+1632C>G
XM_011522170.1:c.372-2598C>G	XP_011520472.1:n.372-2598C>G
XM_011522171.1:c.312-2598C>G	XP_011520473.1:n.312-2598C>G
XM_011522172.1:c.312-2598C>G	XP_011520474.1:n.312-2598C>G
XM_011522173.1:c.312-2598C>G	XP_011520475.1:n.312-2598C>G
XR_931936.1:n.1428C>G
XR_931937.1:n.1371C>G
XR_931938.1:n.1345+516C>G
XR_931939.1:n.1248+1632C>G
XR_931940.1:n.1070-2598C>G
NM_001321135.1:c.872+482C>G	NP_001308064.1:n.872+482C>G
NM_001321136.1:c.860C>G	NP_001308065.1:p.Thr287Ser
NM_001321137.1:c.1082C>G	NP_001308066.1:p.Thr361Ser
NM_003978.4:c.887C>G	NP_003969.2:p.Thr296Ser
NR_135552.1:n.1150+1632C>G
XM_006720737.3:c.521C>G	XP_006720800.1:p.Thr174Ser
XM_011522163.2:c.944C>G	XP_011520465.1:p.Thr315Ser
XM_011522165.2:c.740C>G	XP_011520467.1:p.Thr247Ser
XM_011522166.2:c.978C>G	XP_011520468.1:p.Asp326Glu
XM_011522167.2:c.895+516C>G	XP_011520469.1:n.895+516C>G
XM_011522168.3:c.944C>G	XP_011520470.1:p.Thr315Ser
XM_011522169.2:c.798+1632C>G	XP_011520471.1:n.798+1632C>G
XR_931936.2:n.1426C>G
XR_931937.2:n.1369C>G
XR_931938.2:n.1343+516C>G
XR_931939.2:n.1246+1632C>G
NM_001321135.2:c.872+482C>G	NP_001308064.1:n.872+482C>G
NM_001321136.2:c.860C>G	NP_001308065.1:p.Thr287Ser
NM_003978.5:c.887C>G MANE Select	NP_003969.2:p.Thr296Ser
NR_135552.2:n.1109+1632C>G