Canonical Allele Identifier: CA3057487

Gene: SEC24D

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.118815443C>T , CM000666.2:g.118815443C>T	GRCh38
NC_000004.11:g.119736598C>T , CM000666.1:g.119736598C>T	GRCh37
NC_000004.10:g.119956046C>T	NCBI36
NG_042032.1:g.25729G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_014822.4:c.673+8G>A MANE Select	NP_055637.2:n.673+8G>A
ENST00000280551.11:c.673+8G>A MANE Select	ENSP00000280551.6:n.673+8G>A
NM_001318066.1:c.673+8G>A	NP_001304995.1:n.673+8G>A
NM_001318066.2:c.673+8G>A	NP_001304995.1:n.673+8G>A
NM_014822.2:c.673+8G>A	NP_055637.2:n.673+8G>A
NM_014822.3:c.673+8G>A	NP_055637.2:n.673+8G>A
ENST00000280551.10:c.673+8G>A	ENSP00000280551.6:n.673+8G>A
ENST00000419654.6:c.-660+8G>A	ENSP00000388324.2:n.-660+8G>A
ENST00000506622.5:c.780+8G>A	ENSP00000427249.1:n.780+8G>A
ENST00000509818.5:c.524+8G>A	ENSP00000424085.1:n.524+8G>A
ENST00000514561.5:c.*647+8G>A	ENSP00000422717.1:n.*647+8G>A
XM_005263378.1:c.673+8G>A	XP_005263435.1:n.673+8G>A
XM_005263379.1:c.673+8G>A	XP_005263436.1:n.673+8G>A
XM_005263379.3:c.673+8G>A	XP_005263436.1:n.673+8G>A
XM_011532435.1:c.673+8G>A	XP_011530737.1:n.673+8G>A
XM_011532436.1:c.673+8G>A	XP_011530738.1:n.673+8G>A
XM_024454293.1:c.673+8G>A	XP_024310061.1:n.673+8G>A