Canonical Allele Identifier: CA2130612116

Gene: SEC23A

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.39067228G= , CM000676.2:g.39067228G=	GRCh38
NC_000014.8:g.39536432G= , CM000676.1:g.39536432G=	GRCh37
NC_000014.7:g.38606183G=	NCBI36
NG_012157.1:g.41006C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307712.11:c.1172C= MANE Select	ENSP00000306881.6:p.Thr391=
ENST00000307712.10:c.1172C=	ENSP00000306881.6:p.Thr391=
ENST00000537403.5:c.566C=	ENSP00000444193.1:p.Thr189=
ENST00000545328.6:c.1085C=	ENSP00000445393.2:p.Thr362=
NM_006364.2:c.1172C=	NP_006355.2:p.Thr391=
XM_005267262.1:c.1172C=	XP_005267319.1:p.Thr391=
XM_011536355.1:c.1172C=	XP_011534657.1:p.Thr391=
NM_006364.3:c.1172C=	NP_006355.2:p.Thr391=
XM_005267262.2:c.1172C=	XP_005267319.1:p.Thr391=
XM_011536355.3:c.1172C=	XP_011534657.1:p.Thr391=
XM_017020928.2:c.1172C=	XP_016876417.1:p.Thr391=
NM_006364.4:c.1172C= MANE Select	NP_006355.2:p.Thr391=