Canonical Allele Identifier: CA389535270
Gene: SEC23A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.39067262A>C , CM000676.2:g.39067262A>C GRCh38
NC_000014.8:g.39536466A>C , CM000676.1:g.39536466A>C GRCh37
NC_000014.7:g.38606217A>C NCBI36
NG_012157.1:g.40972T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000307712.11:c.1138T>G MANE Select ENSP00000306881.6:p.Ser380Ala
ENST00000307712.10:c.1138T>G ENSP00000306881.6:p.Ser380Ala
ENST00000537403.5:c.532T>G ENSP00000444193.1:p.Ser178Ala
ENST00000545328.6:c.1051T>G ENSP00000445393.2:p.Ser351Ala
NM_006364.2:c.1138T>G NP_006355.2:p.Ser380Ala
XM_005267262.1:c.1138T>G XP_005267319.1:p.Ser380Ala
XM_011536355.1:c.1138T>G XP_011534657.1:p.Ser380Ala
NM_006364.3:c.1138T>G NP_006355.2:p.Ser380Ala
XM_005267262.2:c.1138T>G XP_005267319.1:p.Ser380Ala
XM_011536355.3:c.1138T>G XP_011534657.1:p.Ser380Ala
XM_017020928.2:c.1138T>G XP_016876417.1:p.Ser380Ala
NM_006364.4:c.1138T>G MANE Select NP_006355.2:p.Ser380Ala