Canonical Allele Identifier: CA1488655426

Gene: SEC24D

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.118815522G= , CM000666.2:g.118815522G=	GRCh38
NC_000004.11:g.119736677G= , CM000666.1:g.119736677G=	GRCh37
NC_000004.10:g.119956125G=	NCBI36
NG_042032.1:g.25650C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280551.11:c.602C= MANE Select	ENSP00000280551.6:p.Pro201=
ENST00000280551.10:c.602C=	ENSP00000280551.6:p.Pro201=
ENST00000419654.6:c.-731C=	ENSP00000388324.2:n.-731C=
ENST00000506622.5:c.709C=	ENSP00000427249.1:p.Leu237=
ENST00000509818.5:c.453C=	ENSP00000424085.1:p.Ser151=
ENST00000514561.5:c.*576C=	ENSP00000422717.1:n.*576C=
NM_014822.2:c.602C=	NP_055637.2:p.Pro201=
XM_005263378.1:c.602C=	XP_005263435.1:p.Pro201=
XM_005263379.1:c.602C=	XP_005263436.1:p.Pro201=
XM_011532435.1:c.602C=	XP_011530737.1:p.Pro201=
XM_011532436.1:c.602C=	XP_011530738.1:p.Pro201=
NM_001318066.1:c.602C=	NP_001304995.1:p.Pro201=
NM_014822.3:c.602C=	NP_055637.2:p.Pro201=
XM_005263379.3:c.602C=	XP_005263436.1:p.Pro201=
XM_024454293.1:c.602C=	XP_024310061.1:p.Pro201=
NM_014822.4:c.602C= MANE Select	NP_055637.2:p.Pro201=
NM_001318066.2:c.602C=	NP_001304995.1:p.Pro201=