Canonical Allele Identifier: CA7161934

Gene: SEC23A

Linked Data

• dbSNP Id: rs766557504
• ExAC: 14:39536464 G / A
• gnomAD v2: 14-39536464-G-A
• gnomAD v4: 14-39067260-G-A
• MyVariant Identifiers: chr14:g.39536464G>A (hg19) ; chr14:g.39067260G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.39067260G>A , CM000676.2:g.39067260G>A	GRCh38
NC_000014.8:g.39536464G>A , CM000676.1:g.39536464G>A	GRCh37
NC_000014.7:g.38606215G>A	NCBI36
NG_012157.1:g.40974C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307712.11:c.1140C>T MANE Select	ENSP00000306881.6:p.Ser380=
ENST00000307712.10:c.1140C>T	ENSP00000306881.6:p.Ser380=
ENST00000537403.5:c.534C>T	ENSP00000444193.1:p.Ser178=
ENST00000545328.6:c.1053C>T	ENSP00000445393.2:p.Ser351=
NM_006364.2:c.1140C>T	NP_006355.2:p.Ser380=
XM_005267262.1:c.1140C>T	XP_005267319.1:p.Ser380=
XM_011536355.1:c.1140C>T	XP_011534657.1:p.Ser380=
NM_006364.3:c.1140C>T	NP_006355.2:p.Ser380=
XM_005267262.2:c.1140C>T	XP_005267319.1:p.Ser380=
XM_011536355.3:c.1140C>T	XP_011534657.1:p.Ser380=
XM_017020928.2:c.1140C>T	XP_016876417.1:p.Ser380=
NM_006364.4:c.1140C>T MANE Select	NP_006355.2:p.Ser380=