Canonical Allele Identifier: CA715848600

Gene: PSTPIP1

Linked Data

• dbSNP Id: rs1438074965
• gnomAD v3: 15-77032740-C-CA
• gnomAD v4: 15-77032740-C-CA
• MyVariant Identifiers: chr15:g.77325081_77325082insA (hg19) ; chr15:g.77032740_77032741insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.77032741dup , CM000677.2:g.77032741dup	GRCh38
NC_000015.9:g.77325082dup , CM000677.1:g.77325082dup	GRCh37
NC_000015.8:g.75112137dup	NCBI36
NG_007526.1:g.42618dup , LRG_172:g.42618dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697622.1:n.1884dup
ENST00000697623.1:n.2258-121dup
ENST00000558012.6:c.839-121dup MANE Select	ENSP00000452746.1:n.839-121dup
ENST00000379595.7:c.839-121dup	ENSP00000368914.3:n.839-121dup
ENST00000557995.1:n.503-121dup
ENST00000558012.5:c.839-121dup	ENSP00000452746.1:n.839-121dup
ENST00000558870.1:c.78+347dup
ENST00000559295.5:c.872+313dup	ENSP00000452743.1:n.872+313dup
ENST00000559785.5:c.1068-121dup	ENSP00000452986.1:n.1068-121dup
ENST00000560223.5:c.*941-121dup	ENSP00000454118.1:n.*941-121dup
ENST00000560377.5:n.1426dup
NM_003978.3:c.839-121dup , LRG_172t1:c.839-121dup	NP_003969.2:n.839-121dup
XM_006720737.2:c.473-121dup	XP_006720800.1:n.473-121dup
XM_011522163.1:c.896-121dup	XP_011520465.1:n.896-121dup
XM_011522164.1:c.794-121dup	XP_011520466.1:n.794-121dup
XM_011522165.1:c.692-121dup	XP_011520467.1:n.692-121dup
XM_011522166.1:c.930-121dup	XP_011520468.1:n.930-121dup
XM_011522167.1:c.895+347dup	XP_011520469.1:n.895+347dup
XM_011522168.1:c.896-121dup	XP_011520470.1:n.896-121dup
XM_011522169.1:c.798+1463dup	XP_011520471.1:n.798+1463dup
XM_011522170.1:c.372-2767dup	XP_011520472.1:n.372-2767dup
XM_011522171.1:c.312-2767dup	XP_011520473.1:n.312-2767dup
XM_011522172.1:c.312-2767dup	XP_011520474.1:n.312-2767dup
XM_011522173.1:c.312-2767dup	XP_011520475.1:n.312-2767dup
XR_931936.1:n.1380-121dup
XR_931937.1:n.1323-121dup
XR_931938.1:n.1345+347dup
XR_931939.1:n.1248+1463dup
XR_931940.1:n.1070-2767dup
NM_001321135.1:c.872+313dup	NP_001308064.1:n.872+313dup
NM_001321136.1:c.812-121dup	NP_001308065.1:n.812-121dup
NM_001321137.1:c.1034-121dup	NP_001308066.1:n.1034-121dup
NM_003978.4:c.839-121dup	NP_003969.2:n.839-121dup
NR_135552.1:n.1150+1463dup
XM_006720737.3:c.473-121dup	XP_006720800.1:n.473-121dup
XM_011522163.2:c.896-121dup	XP_011520465.1:n.896-121dup
XM_011522165.2:c.692-121dup	XP_011520467.1:n.692-121dup
XM_011522166.2:c.930-121dup	XP_011520468.1:n.930-121dup
XM_011522167.2:c.895+347dup	XP_011520469.1:n.895+347dup
XM_011522168.3:c.896-121dup	XP_011520470.1:n.896-121dup
XM_011522169.2:c.798+1463dup	XP_011520471.1:n.798+1463dup
XR_931936.2:n.1378-121dup
XR_931937.2:n.1321-121dup
XR_931938.2:n.1343+347dup
XR_931939.2:n.1246+1463dup
NM_001321135.2:c.872+313dup	NP_001308064.1:n.872+313dup
NM_001321136.2:c.812-121dup	NP_001308065.1:n.812-121dup
NM_003978.5:c.839-121dup MANE Select	NP_003969.2:n.839-121dup
NR_135552.2:n.1109+1463dup