Canonical Allele Identifier: CA2130612068

Gene: SEC23A

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.39067185C= , CM000676.2:g.39067185C=	GRCh38
NC_000014.8:g.39536389C= , CM000676.1:g.39536389C=	GRCh37
NC_000014.7:g.38606140C=	NCBI36
NG_012157.1:g.41049G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307712.11:c.1215G= MANE Select	ENSP00000306881.6:p.Thr405=
ENST00000307712.10:c.1215G=	ENSP00000306881.6:p.Thr405=
ENST00000537403.5:c.609G=	ENSP00000444193.1:p.Thr203=
ENST00000545328.6:c.1128G=	ENSP00000445393.2:p.Thr376=
ENST00000553925.1:n.27G=
NM_006364.2:c.1215G=	NP_006355.2:p.Thr405=
XM_005267262.1:c.1215G=	XP_005267319.1:p.Thr405=
XM_011536355.1:c.1215G=	XP_011534657.1:p.Thr405=
NM_006364.3:c.1215G=	NP_006355.2:p.Thr405=
XM_005267262.2:c.1215G=	XP_005267319.1:p.Thr405=
XM_011536355.3:c.1215G=	XP_011534657.1:p.Thr405=
XM_017020928.2:c.1215G=	XP_016876417.1:p.Thr405=
NM_006364.4:c.1215G= MANE Select	NP_006355.2:p.Thr405=