Canonical Allele Identifier: CA7161921
Gene: SEC23A HGNC NCBI

Linked Data

dbSNP Id: rs755662503

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.39067186G>A , CM000676.2:g.39067186G>A GRCh38
NC_000014.8:g.39536390G>A , CM000676.1:g.39536390G>A GRCh37
NC_000014.7:g.38606141G>A NCBI36
NG_012157.1:g.41048C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000307712.11:c.1214C>T MANE Select ENSP00000306881.6:p.Thr405Met
ENST00000307712.10:c.1214C>T ENSP00000306881.6:p.Thr405Met
ENST00000537403.5:c.608C>T ENSP00000444193.1:p.Thr203Met
ENST00000545328.6:c.1127C>T ENSP00000445393.2:p.Thr376Met
ENST00000553925.1:n.26C>T
NM_006364.2:c.1214C>T NP_006355.2:p.Thr405Met
XM_005267262.1:c.1214C>T XP_005267319.1:p.Thr405Met
XM_011536355.1:c.1214C>T XP_011534657.1:p.Thr405Met
NM_006364.3:c.1214C>T NP_006355.2:p.Thr405Met
XM_005267262.2:c.1214C>T XP_005267319.1:p.Thr405Met
XM_011536355.3:c.1214C>T XP_011534657.1:p.Thr405Met
XM_017020928.2:c.1214C>T XP_016876417.1:p.Thr405Met
NM_006364.4:c.1214C>T MANE Select NP_006355.2:p.Thr405Met