Canonical Allele Identifier: CA389535122

Gene: SEC23A

Linked Data

• MyVariant Identifiers: chr14:g.39536402C>A (hg19) ; chr14:g.39067198C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.39067198C>A , CM000676.2:g.39067198C>A	GRCh38
NC_000014.8:g.39536402C>A , CM000676.1:g.39536402C>A	GRCh37
NC_000014.7:g.38606153C>A	NCBI36
NG_012157.1:g.41036G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307712.11:c.1202G>T MANE Select	ENSP00000306881.6:p.Gly401Val
ENST00000307712.10:c.1202G>T	ENSP00000306881.6:p.Gly401Val
ENST00000537403.5:c.596G>T	ENSP00000444193.1:p.Gly199Val
ENST00000545328.6:c.1115G>T	ENSP00000445393.2:p.Gly372Val
ENST00000553925.1:n.14G>T
NM_006364.2:c.1202G>T	NP_006355.2:p.Gly401Val
XM_005267262.1:c.1202G>T	XP_005267319.1:p.Gly401Val
XM_011536355.1:c.1202G>T	XP_011534657.1:p.Gly401Val
NM_006364.3:c.1202G>T	NP_006355.2:p.Gly401Val
XM_005267262.2:c.1202G>T	XP_005267319.1:p.Gly401Val
XM_011536355.3:c.1202G>T	XP_011534657.1:p.Gly401Val
XM_017020928.2:c.1202G>T	XP_016876417.1:p.Gly401Val
NM_006364.4:c.1202G>T MANE Select	NP_006355.2:p.Gly401Val