Canonical Allele Identifier: CA303960541
Gene: PTBP1 HGNC NCBI

Linked Data

dbSNP Id: rs945966565
gnomAD v3: 19-801418-A-T
gnomAD v4: 19-801418-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.801418A>T , CM000681.2:g.801418A>T GRCh38
NC_000019.9:g.801418A>T , CM000681.1:g.801418A>T GRCh37
NC_000019.8:g.752418A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000356948.11:c.39+1975A>T MANE Select ENSP00000349428.4:n.39+1975A>T
ENST00000592804.2:n.139+1975A>T
ENST00000676227.1:c.39+1975A>T ENSP00000501551.1:n.39+1975A>T
ENST00000677277.1:c.39+1975A>T ENSP00000504032.1:n.39+1975A>T
ENST00000679114.1:c.45+1975A>T ENSP00000504829.1:n.45+1975A>T
ENST00000349038.8:c.39+1975A>T ENSP00000014112.5:n.39+1975A>T
ENST00000350092.8:c.-52+1975A>T ENSP00000342332.5:n.-52+1975A>T
ENST00000356948.10:c.39+1975A>T ENSP00000349428.4:n.39+1975A>T
ENST00000394601.8:c.39+1975A>T ENSP00000408096.1:n.39+1975A>T
ENST00000586481.5:c.-51-2143A>T ENSP00000468565.3:n.-51-2143A>T
ENST00000586944.5:n.109+1975A>T
ENST00000587094.2:c.45+1975A>T ENSP00000465825.1:n.45+1975A>T
ENST00000587191.3:c.-66+1975A>T ENSP00000478974.1:n.-66+1975A>T
ENST00000589575.5:c.39+1975A>T ENSP00000465652.2:n.39+1975A>T
ENST00000590887.5:n.112+1975A>T
ENST00000627714.2:c.39+1975A>T ENSP00000486218.1:n.39+1975A>T
ENST00000635647.1:c.39+1975A>T ENSP00000489604.1:n.39+1975A>T
NM_002819.4:c.39+1975A>T NP_002810.1:n.39+1975A>T
NM_031990.3:c.39+1975A>T NP_114367.1:n.39+1975A>T
NM_031991.3:c.39+1975A>T NP_114368.1:n.39+1975A>T
XM_005259597.2:c.45+1975A>T XP_005259654.1:n.45+1975A>T
XM_005259598.2:c.45+1975A>T XP_005259655.1:n.45+1975A>T
XR_244034.2:n.648+1975A>T
XR_244035.2:n.648+1975A>T
NM_002819.5:c.39+1975A>T MANE Select NP_002810.1:n.39+1975A>T
NM_031990.4:c.39+1975A>T NP_114367.1:n.39+1975A>T
NM_031991.4:c.39+1975A>T NP_114368.1:n.39+1975A>T