Canonical Allele Identifier: CA393521996
Gene: PSTPIP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.77037082T>A , CM000677.2:g.77037082T>A GRCh38
NC_000015.9:g.77329423T>A , CM000677.1:g.77329423T>A GRCh37
NC_000015.8:g.75116478T>A NCBI36
NG_007526.1:g.46959T>A , LRG_172:g.46959T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000697622.1:n.2323T>A
ENST00000697623.1:n.2576T>A
ENST00000558012.6:c.1157T>A MANE Select ENSP00000452746.1:p.Leu386Gln
ENST00000379595.7:c.1148T>A ENSP00000368914.3:p.Leu383Gln
ENST00000557995.1:n.821T>A
ENST00000558012.5:c.1157T>A ENSP00000452746.1:p.Leu386Gln
ENST00000558870.1:c.306T>A
ENST00000559295.5:c.1100T>A ENSP00000452743.1:p.Leu367Gln
ENST00000559785.5:c.*132T>A ENSP00000452986.1:n.*132T>A
ENST00000560064.1:n.280T>A
ENST00000560223.5:c.*1259T>A ENSP00000454118.1:n.*1259T>A
NM_003978.3:c.1157T>A , LRG_172t1:c.1157T>A NP_003969.2:p.Leu386Gln
XM_006720737.2:c.791T>A XP_006720800.1:p.Leu264Gln
XM_011522163.1:c.1205T>A XP_011520465.1:p.Leu402Gln
XM_011522164.1:c.1112T>A XP_011520466.1:p.Leu371Gln
XM_011522165.1:c.1010T>A XP_011520467.1:p.Leu337Gln
XM_011522168.1:c.1214T>A XP_011520470.1:p.Leu405Gln
XM_011522170.1:c.599T>A XP_011520472.1:p.Leu200Gln
XM_011522171.1:c.539T>A XP_011520473.1:p.Leu180Gln
XM_011522172.1:c.539T>A XP_011520474.1:p.Leu180Gln
XM_011522173.1:c.539T>A XP_011520475.1:p.Leu180Gln
XR_931936.1:n.1698T>A
XR_931937.1:n.1641T>A
XR_931938.1:n.1573T>A
XR_931939.1:n.1476T>A
XR_931940.1:n.1297T>A
NM_001321135.1:c.1100T>A NP_001308064.1:p.Leu367Gln
NM_001321136.1:c.1130T>A NP_001308065.1:p.Leu377Gln
NM_001321137.1:c.1352T>A NP_001308066.1:p.Leu451Gln
NM_003978.4:c.1157T>A NP_003969.2:p.Leu386Gln
NR_135552.1:n.1378T>A
XM_006720737.3:c.791T>A XP_006720800.1:p.Leu264Gln
XM_011522163.2:c.1205T>A XP_011520465.1:p.Leu402Gln
XM_011522165.2:c.1010T>A XP_011520467.1:p.Leu337Gln
XM_011522168.3:c.1214T>A XP_011520470.1:p.Leu405Gln
XR_931936.2:n.1696T>A
XR_931937.2:n.1639T>A
XR_931938.2:n.1571T>A
XR_931939.2:n.1474T>A
NM_001321135.2:c.1100T>A NP_001308064.1:p.Leu367Gln
NM_001321136.2:c.1130T>A NP_001308065.1:p.Leu377Gln
NM_003978.5:c.1157T>A MANE Select NP_003969.2:p.Leu386Gln
NR_135552.2:n.1337T>A