Canonical Allele Identifier: CA2697554318
Community Standard Title: NM_001321759.2(CDIN1):c.260_263del (p.Asp87GlyfsTer11)
Gene: CDIN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.36654145_36654148del , CM000677.2:g.36654145_36654148del GRCh38
NC_000015.9:g.36946346_36946349del , CM000677.1:g.36946346_36946349del GRCh37
NC_000015.8:g.34733638_34733641del NCBI36
NG_034055.1:g.79543_79546del

Transcript Alleles

HGVS Amino-acid Change
NM_001321759.2:c.260_263del MANE Select NP_001308688.1:p.Asp87GlyfsTer11
ENST00000566621.6:c.260_263del MANE Select ENSP00000455397.1:p.Asp87GlyfsTer11
NM_001130010.2:c.260_263del NP_001123482.1:p.Asp87GlyfsTer11
NM_001130010.3:c.260_263del NP_001123482.1:p.Asp87GlyfsTer11
NM_001290232.1:c.-35_-32del NP_001277161.1:n.-35_-32del
NM_001290232.2:c.-35_-32del NP_001277161.1:n.-35_-32del
NM_001290233.1:c.260_263del NP_001277162.1:p.Asp87GlyfsTer11
NM_001290233.2:c.260_263del NP_001277162.1:p.Asp87GlyfsTer11
NM_001321756.1:c.-35_-32del NP_001308685.1:n.-35_-32del
NM_001321756.2:c.-35_-32del NP_001308685.1:n.-35_-32del
NM_001321757.1:c.-144_-141del NP_001308686.1:n.-144_-141del
NM_001321757.2:c.-144_-141del NP_001308686.1:n.-144_-141del
NM_001321758.1:c.149_152del NP_001308687.1:p.Asp50GlyfsTer11
NM_001321758.2:c.149_152del NP_001308687.1:p.Asp50GlyfsTer11
NM_001321759.1:c.260_263del NP_001308688.1:p.Asp87GlyfsTer11
NM_001321760.1:c.260_263del NP_001308689.1:p.Asp87GlyfsTer11
NM_001321760.2:c.260_263del NP_001308689.1:p.Asp87GlyfsTer11
NM_001321761.1:c.260_263del NP_001308690.1:p.Asp87GlyfsTer11
NM_001321761.2:c.260_263del NP_001308690.1:p.Asp87GlyfsTer11
NM_032499.5:c.-35_-32del NP_115888.1:n.-35_-32del
NM_032499.6:c.-35_-32del NP_115888.1:n.-35_-32del
ENST00000338183.8:c.-35_-32del ENSP00000342433.4:n.-35_-32del
ENST00000437989.6:c.260_263del ENSP00000401362.2:p.Asp87GlyfsTer11
ENST00000562877.5:c.-35_-32del ENSP00000457854.1:n.-35_-32del
ENST00000564586.5:c.149_152del ENSP00000457227.1:p.Asp50GlyfsTer11
ENST00000566621.5:c.260_263del ENSP00000455397.1:p.Asp87GlyfsTer11
ENST00000566807.5:c.-35_-32del ENSP00000454831.1:n.-35_-32del
ENST00000567389.5:c.-35_-32del ENSP00000456736.1:n.-35_-32del
ENST00000569302.5:c.260_263del ENSP00000456477.1:p.Asp87GlyfsTer11
ENST00000569302.6:c.260_263del ENSP00000456477.1:p.Asp87GlyfsTer11
ENST00000570265.5:n.487_490del
ENST00000570265.6:c.260_263del ENSP00000493669.1:p.Asp87GlyfsTer11
ENST00000642817.1:c.*40_*43del ENSP00000495947.1:n.*40_*43del
ENST00000643612.1:c.-219_-216del ENSP00000496325.1:n.-219_-216del
ENST00000643822.1:c.*245_*248del ENSP00000493719.1:n.*245_*248del
ENST00000643837.1:n.434_437del
ENST00000646533.1:c.260_263del ENSP00000494718.1:p.Asp87GlyfsTer11
ENST00000646657.1:c.260_263del ENSP00000495542.1:p.Asp87GlyfsTer11
ENST00000647059.1:n.53_56del
XM_011522110.1:c.260_263del XP_011520412.1:p.Asp87GlyfsTer11
XM_011522111.1:c.260_263del XP_011520413.1:p.Asp87GlyfsTer11
XM_011522112.1:c.-35_-32del XP_011520414.1:n.-35_-32del
XM_017022676.1:c.260_263del XP_016878165.1:p.Asp87GlyfsTer11
XM_017022677.1:c.260_263del XP_016878166.1:p.Asp87GlyfsTer11
XM_024450088.1:c.-35_-32del XP_024305856.1:n.-35_-32del
XR_002957689.1:n.510_513del
XR_931921.1:n.510_513del
XR_931922.1:n.510_513del
XR_931923.1:n.510_513del
XR_931924.1:n.510_513del