Canonical Allele Identifier: CA2225119841

Gene: CNOT1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.58533367_58533368delinsTG , CM000678.2:g.58533367_58533368delinsTG	GRCh38
NC_000016.9:g.58567271_58567272delinsTG , CM000678.1:g.58567271_58567272delinsTG	GRCh37
NC_000016.8:g.57124772_57124773delinsTG	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000317147.10:c.5895+779_5895+780delinsCA MANE Select	ENSP00000320949.5:n.5895+779_5895+780deli...
ENST00000317147.9:c.5895+779_5895+780delinsCA	ENSP00000320949.5:n.5895+779_5895+780deli...
ENST00000567188.5:c.5880+779_5880+780delinsCA	ENSP00000456649.1:n.5880+779_5880+780deli...
ENST00000568917.1:c.1035+779_1035+780delinsCA	ENSP00000454611.1:n.1035+779_1035+780deli...
ENST00000569240.5:c.5880+779_5880+780delinsCA	ENSP00000455635.1:n.5880+779_5880+780deli...
NM_001265612.1:c.5880+779_5880+780delinsCA	NP_001252541.1:n.5880+779_5880+780delinsC...
NM_016284.4:c.5895+779_5895+780delinsCA	NP_057368.3:n.5895+779_5895+780delinsCA
NR_049763.1:n.6213+779_6213+780delinsCA
NM_016284.5:c.5895+779_5895+780delinsCA MANE Select	NP_057368.3:n.5895+779_5895+780delinsCA
NM_001265612.2:c.5880+779_5880+780delinsCA	NP_001252541.1:n.5880+779_5880+780delinsC...
NR_049763.2:n.6153+779_6153+780delinsCA