Canonical Allele Identifier: CA389535115

Gene: SEC23A

Linked Data

• MyVariant Identifiers: chr14:g.39536399A>G (hg19) ; chr14:g.39067195A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.39067195A>G , CM000676.2:g.39067195A>G	GRCh38
NC_000014.8:g.39536399A>G , CM000676.1:g.39536399A>G	GRCh37
NC_000014.7:g.38606150A>G	NCBI36
NG_012157.1:g.41039T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307712.11:c.1205T>C MANE Select	ENSP00000306881.6:p.Phe402Ser
ENST00000307712.10:c.1205T>C	ENSP00000306881.6:p.Phe402Ser
ENST00000537403.5:c.599T>C	ENSP00000444193.1:p.Phe200Ser
ENST00000545328.6:c.1118T>C	ENSP00000445393.2:p.Phe373Ser
ENST00000553925.1:n.17T>C
NM_006364.2:c.1205T>C	NP_006355.2:p.Phe402Ser
XM_005267262.1:c.1205T>C	XP_005267319.1:p.Phe402Ser
XM_011536355.1:c.1205T>C	XP_011534657.1:p.Phe402Ser
NM_006364.3:c.1205T>C	NP_006355.2:p.Phe402Ser
XM_005267262.2:c.1205T>C	XP_005267319.1:p.Phe402Ser
XM_011536355.3:c.1205T>C	XP_011534657.1:p.Phe402Ser
XM_017020928.2:c.1205T>C	XP_016876417.1:p.Phe402Ser
NM_006364.4:c.1205T>C MANE Select	NP_006355.2:p.Phe402Ser