Canonical Allele Identifier: CA7161936
Gene: SEC23A HGNC NCBI

Linked Data

dbSNP Id: rs199838604

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.39067267T>G , CM000676.2:g.39067267T>G GRCh38
NC_000014.8:g.39536471T>G , CM000676.1:g.39536471T>G GRCh37
NC_000014.7:g.38606222T>G NCBI36
NG_012157.1:g.40967A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000307712.11:c.1133A>C MANE Select ENSP00000306881.6:p.Asn378Thr
ENST00000307712.10:c.1133A>C ENSP00000306881.6:p.Asn378Thr
ENST00000537403.5:c.527A>C ENSP00000444193.1:p.Asn176Thr
ENST00000545328.6:c.1046A>C ENSP00000445393.2:p.Asn349Thr
NM_006364.2:c.1133A>C NP_006355.2:p.Asn378Thr
XM_005267262.1:c.1133A>C XP_005267319.1:p.Asn378Thr
XM_011536355.1:c.1133A>C XP_011534657.1:p.Asn378Thr
NM_006364.3:c.1133A>C NP_006355.2:p.Asn378Thr
XM_005267262.2:c.1133A>C XP_005267319.1:p.Asn378Thr
XM_011536355.3:c.1133A>C XP_011534657.1:p.Asn378Thr
XM_017020928.2:c.1133A>C XP_016876417.1:p.Asn378Thr
NM_006364.4:c.1133A>C MANE Select NP_006355.2:p.Asn378Thr