Canonical Allele Identifier: CA2317325902

Gene: PTBP1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.801332_801335delinsTCTG , CM000681.2:g.801332_801335delinsTCTG	GRCh38
NC_000019.9:g.801332_801335delinsTCTG , CM000681.1:g.801332_801335delinsTCTG	GRCh37
NC_000019.8:g.752332_752335delinsTCTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356948.11:c.39+1889_39+1892delinsTCTG MANE Select	ENSP00000349428.4:n.39+1889_39+1892delinsTCTG
ENST00000592804.2:n.139+1889_139+1892delinsTCTG
ENST00000676227.1:c.39+1889_39+1892delinsTCTG	ENSP00000501551.1:n.39+1889_39+1892delinsTCTG
ENST00000677277.1:c.39+1889_39+1892delinsTCTG	ENSP00000504032.1:n.39+1889_39+1892delinsTCTG
ENST00000679114.1:c.45+1889_45+1892delinsTCTG	ENSP00000504829.1:n.45+1889_45+1892delinsTCTG
ENST00000349038.8:c.39+1889_39+1892delinsTCTG	ENSP00000014112.5:n.39+1889_39+1892delinsTCTG
ENST00000350092.8:c.-52+1889_-52+1892delinsTCTG	ENSP00000342332.5:n.-52+1889_-52+1892delinsTCTG
ENST00000356948.10:c.39+1889_39+1892delinsTCTG	ENSP00000349428.4:n.39+1889_39+1892delinsTCTG
ENST00000394601.8:c.39+1889_39+1892delinsTCTG	ENSP00000408096.1:n.39+1889_39+1892delinsTCTG
ENST00000586481.5:c.-51-2229_-51-2226delinsTCTG	ENSP00000468565.3:n.-51-2229_-51-2226delinsTCTG
ENST00000586944.5:n.109+1889_109+1892delinsTCTG
ENST00000587094.2:c.45+1889_45+1892delinsTCTG	ENSP00000465825.1:n.45+1889_45+1892delinsTCTG
ENST00000587191.3:c.-66+1889_-66+1892delinsTCTG	ENSP00000478974.1:n.-66+1889_-66+1892delinsTCTG
ENST00000589575.5:c.39+1889_39+1892delinsTCTG	ENSP00000465652.2:n.39+1889_39+1892delinsTCTG
ENST00000590887.5:n.112+1889_112+1892delinsTCTG
ENST00000627714.2:c.39+1889_39+1892delinsTCTG	ENSP00000486218.1:n.39+1889_39+1892delinsTCTG
ENST00000635647.1:c.39+1889_39+1892delinsTCTG	ENSP00000489604.1:n.39+1889_39+1892delinsTCTG
NM_002819.4:c.39+1889_39+1892delinsTCTG	NP_002810.1:n.39+1889_39+1892delinsTCTG
NM_031990.3:c.39+1889_39+1892delinsTCTG	NP_114367.1:n.39+1889_39+1892delinsTCTG
NM_031991.3:c.39+1889_39+1892delinsTCTG	NP_114368.1:n.39+1889_39+1892delinsTCTG
XM_005259597.2:c.45+1889_45+1892delinsTCTG	XP_005259654.1:n.45+1889_45+1892delinsTCTG
XM_005259598.2:c.45+1889_45+1892delinsTCTG	XP_005259655.1:n.45+1889_45+1892delinsTCTG
XR_244034.2:n.648+1889_648+1892delinsTCTG
XR_244035.2:n.648+1889_648+1892delinsTCTG
NM_002819.5:c.39+1889_39+1892delinsTCTG MANE Select	NP_002810.1:n.39+1889_39+1892delinsTCTG
NM_031990.4:c.39+1889_39+1892delinsTCTG	NP_114367.1:n.39+1889_39+1892delinsTCTG
NM_031991.4:c.39+1889_39+1892delinsTCTG	NP_114368.1:n.39+1889_39+1892delinsTCTG