Canonical Allele Identifier: CA1488623083

Gene: SEC24D

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.118739143_118739162dup , CM000666.2:g.118739143_118739162dup	GRCh38
NC_000004.11:g.119660298_119660317dup , CM000666.1:g.119660298_119660317dup	GRCh37
NC_000004.10:g.119879746_119879765dup	NCBI36
NG_042032.1:g.102019_102038dup

Transcript Alleles

HGVS	Amino-acid Change
NM_001318066.1:c.2376_2380+15dup
NM_001318066.2:c.2376_2380+15dup
NM_014822.2:c.2373_2377+15dup
NM_014822.3:c.2373_2377+15dup
NM_014822.4:c.2373_2377+15dup
ENST00000280551.10:c.2373_2377+15dup
ENST00000280551.11:c.2373_2377+15dup
ENST00000419654.6:c.1041_1045+15dup
ENST00000502526.1:n.71_75+15dup
ENST00000505134.5:n.1661_1665+15dup
ENST00000511481.5:c.1266_1270+15dup
ENST00000514561.5:c.*2780_*2784+15dup
XM_005263378.1:c.2376_2380+15dup
XM_005263379.1:c.2376_2380+15dup
XM_005263379.3:c.2376_2380+15dup
XM_011532435.1:c.2376_2380+15dup
XM_011532436.1:c.2376_2380+15dup
XM_011532437.1:c.1041_1045+15dup
XM_017008875.1:c.1041_1045+15dup
XM_024454293.1:c.2373_2377+15dup