Canonical Allele Identifier: CA389537784

Gene: SEC23A

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.39096004C>T , CM000676.2:g.39096004C>T	GRCh38
NC_000014.8:g.39565208C>T , CM000676.1:g.39565208C>T	GRCh37
NC_000014.7:g.38634959C>T	NCBI36
NG_012157.1:g.12230G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_006364.4:c.115G>A MANE Select	NP_006355.2:p.Ala39Thr
ENST00000307712.11:c.115G>A MANE Select	ENSP00000306881.6:p.Ala39Thr
NM_006364.2:c.115G>A	NP_006355.2:p.Ala39Thr
NM_006364.3:c.115G>A	NP_006355.2:p.Ala39Thr
ENST00000307712.10:c.115G>A	ENSP00000306881.6:p.Ala39Thr
ENST00000545328.6:c.115G>A	ENSP00000445393.2:p.Ala39Thr
ENST00000548032.6:c.115G>A	ENSP00000447489.2:p.Ala39Thr
ENST00000553970.1:c.115G>A	ENSP00000451924.1:p.Ala39Thr
ENST00000555017.5:c.115G>A	ENSP00000450819.1:p.Ala39Thr
ENST00000555425.5:c.115G>A	ENSP00000451999.1:p.Ala39Thr
ENST00000556092.5:c.115G>A	ENSP00000451230.1:p.Ala39Thr
ENST00000557280.5:c.115G>A	ENSP00000452575.1:p.Ala39Thr
ENST00000557437.1:c.115G>A	ENSP00000452390.1:p.Ala39Thr
ENST00000625395.1:c.115G>A	ENSP00000486142.1:p.Ala39Thr
XM_005267262.1:c.115G>A	XP_005267319.1:p.Ala39Thr
XM_005267262.2:c.115G>A	XP_005267319.1:p.Ala39Thr
XM_011536355.1:c.115G>A	XP_011534657.1:p.Ala39Thr
XM_011536355.3:c.115G>A	XP_011534657.1:p.Ala39Thr
XM_017020928.2:c.115G>A	XP_016876417.1:p.Ala39Thr