Canonical Allele Identifier: CA2652042672
Gene: SEC23B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.18526595_18526596del , CM000682.2:g.18526595_18526596del GRCh38
NC_000020.10:g.18507239_18507240del , CM000682.1:g.18507239_18507240del GRCh37
NC_000020.9:g.18455239_18455240del NCBI36
NG_016281.1:g.24052_24053del
NG_016281.2:g.24114_24115del

Transcript Alleles

HGVS Amino-acid Change
ENST00000336714.8:c.993+64_993+65del ENSP00000338844.3:n.993+64_993+65del
ENST00000377465.6:c.993+64_993+65del ENSP00000366685.1:n.993+64_993+65del
ENST00000643747.1:c.939+64_939+65del ENSP00000496460.1:n.939+64_939+65del
ENST00000650089.1:c.993+64_993+65del MANE Select ENSP00000497473.1:n.993+64_993+65del
ENST00000262544.6:c.993+64_993+65del ENSP00000262544.2:n.993+64_993+65del
ENST00000336714.7:c.993+64_993+65del ENSP00000338844.3:n.993+64_993+65del
ENST00000377465.5:c.993+64_993+65del ENSP00000366685.1:n.993+64_993+65del
ENST00000377475.7:c.993+64_993+65del ENSP00000366695.3:n.993+64_993+65del
NM_001172745.1:c.993+64_993+65del NP_001166216.1:n.993+64_993+65del
NM_001172746.1:c.939+64_939+65del NP_001166217.1:n.939+64_939+65del
NM_006363.4:c.993+64_993+65del NP_006354.2:n.993+64_993+65del
NM_032985.4:c.993+64_993+65del NP_116780.1:n.993+64_993+65del
NM_032986.3:c.993+64_993+65del NP_116781.1:n.993+64_993+65del
NM_001172745.2:c.993+64_993+65del NP_001166216.1:n.993+64_993+65del
NM_001172746.2:c.939+64_939+65del NP_001166217.1:n.939+64_939+65del
NM_006363.6:c.993+64_993+65del MANE Select NP_006354.2:n.993+64_993+65del
NM_032985.5:c.993+64_993+65del NP_116780.1:n.993+64_993+65del
NM_032986.4:c.993+64_993+65del NP_116781.1:n.993+64_993+65del
XM_017027593.1:c.993+64_993+65del XP_016883082.1:n.993+64_993+65del
NM_001172745.3:c.993+64_993+65del NP_001166216.1:n.993+64_993+65del
NM_001172746.3:c.939+64_939+65del NP_001166217.1:n.939+64_939+65del
NM_032985.6:c.993+64_993+65del NP_116780.1:n.993+64_993+65del
NM_032986.5:c.993+64_993+65del NP_116781.1:n.993+64_993+65del