Canonical Allele Identifier: CA3057114

Gene: SEC24D

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.118744054G>A , CM000666.2:g.118744054G>A	GRCh38
NC_000004.11:g.119665209G>A , CM000666.1:g.119665209G>A	GRCh37
NC_000004.10:g.119884657G>A	NCBI36
NG_042032.1:g.97118C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280551.11:c.1929C>T MANE Select	ENSP00000280551.6:p.Asp643=
ENST00000280551.10:c.1929C>T	ENSP00000280551.6:p.Asp643=
ENST00000419654.6:c.597C>T	ENSP00000388324.2:p.Asp199=
ENST00000505134.5:n.1217C>T
ENST00000511481.5:c.822C>T	ENSP00000425491.1:p.Asp274=
ENST00000514561.5:c.*2336C>T	ENSP00000422717.1:n.*2336C>T
NM_014822.2:c.1929C>T	NP_055637.2:p.Asp643=
XM_005263378.1:c.1932C>T	XP_005263435.1:p.Asp644=
XM_005263379.1:c.1932C>T	XP_005263436.1:p.Asp644=
XM_011532435.1:c.1932C>T	XP_011530737.1:p.Asp644=
XM_011532436.1:c.1932C>T	XP_011530738.1:p.Asp644=
XM_011532437.1:c.597C>T	XP_011530739.1:p.Asp199=
NM_001318066.1:c.1932C>T	NP_001304995.1:p.Asp644=
NM_014822.3:c.1929C>T	NP_055637.2:p.Asp643=
XM_005263379.3:c.1932C>T	XP_005263436.1:p.Asp644=
XM_017008875.1:c.597C>T	XP_016864364.1:p.Asp199=
XM_024454293.1:c.1929C>T	XP_024310061.1:p.Asp643=
NM_014822.4:c.1929C>T MANE Select	NP_055637.2:p.Asp643=
NM_001318066.2:c.1932C>T	NP_001304995.1:p.Asp644=