Canonical Allele Identifier: CA486103580

Gene: SEC23A

Linked Data

• MyVariant Identifiers: chr14:g.39536434A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.39067230A>G , CM000676.2:g.39067230A>G	GRCh38
NC_000014.8:g.39536434A>G , CM000676.1:g.39536434A>G	GRCh37
NC_000014.7:g.38606185A>G	NCBI36
NG_012157.1:g.41004T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307712.11:c.1170T>C MANE Select	ENSP00000306881.6:p.Phe390=
ENST00000307712.10:c.1170T>C	ENSP00000306881.6:p.Phe390=
ENST00000537403.5:c.564T>C	ENSP00000444193.1:p.Phe188=
ENST00000545328.6:c.1083T>C	ENSP00000445393.2:p.Phe361=
NM_006364.2:c.1170T>C	NP_006355.2:p.Phe390=
XM_005267262.1:c.1170T>C	XP_005267319.1:p.Phe390=
XM_011536355.1:c.1170T>C	XP_011534657.1:p.Phe390=
NM_006364.3:c.1170T>C	NP_006355.2:p.Phe390=
XM_005267262.2:c.1170T>C	XP_005267319.1:p.Phe390=
XM_011536355.3:c.1170T>C	XP_011534657.1:p.Phe390=
XM_017020928.2:c.1170T>C	XP_016876417.1:p.Phe390=
NM_006364.4:c.1170T>C MANE Select	NP_006355.2:p.Phe390=