Canonical Allele Identifier: CA2130612159
Gene: SEC23A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.39067259_39067260delinsAG , CM000676.2:g.39067259_39067260delinsAG GRCh38
NC_000014.8:g.39536463_39536464delinsAG , CM000676.1:g.39536463_39536464delinsAG GRCh37
NC_000014.7:g.38606214_38606215delinsAG NCBI36
NG_012157.1:g.40974_40975delinsCT

Transcript Alleles

HGVS Amino-acid change
ENST00000307712.11:c.1140_1141delinsCT MANE Select ENSP00000306881.6:p.Ser380=
ENST00000307712.10:c.1140_1141delinsCT ENSP00000306881.6:p.Ser380=
ENST00000537403.5:c.534_535delinsCT ENSP00000444193.1:p.Ser178=
ENST00000545328.6:c.1053_1054delinsCT ENSP00000445393.2:p.Ser351=
NM_006364.2:c.1140_1141delinsCT NP_006355.2:p.Ser380=
XM_005267262.1:c.1140_1141delinsCT XP_005267319.1:p.Ser380=
XM_011536355.1:c.1140_1141delinsCT XP_011534657.1:p.Ser380=
NM_006364.3:c.1140_1141delinsCT NP_006355.2:p.Ser380=
XM_005267262.2:c.1140_1141delinsCT XP_005267319.1:p.Ser380=
XM_011536355.3:c.1140_1141delinsCT XP_011534657.1:p.Ser380=
XM_017020928.2:c.1140_1141delinsCT XP_016876417.1:p.Ser380=
NM_006364.4:c.1140_1141delinsCT MANE Select NP_006355.2:p.Ser380=