Canonical Allele Identifier: CA104657244

Gene: SEC24D

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.118814806del , CM000666.2:g.118814806del	GRCh38
NC_000004.11:g.119735961del , CM000666.1:g.119735961del	GRCh37
NC_000004.10:g.119955409del	NCBI36
NG_042032.1:g.26375del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280551.11:c.801+231del MANE Select	ENSP00000280551.6:n.801+231del
ENST00000280551.10:c.801+231del	ENSP00000280551.6:n.801+231del
ENST00000419654.6:c.-532+231del	ENSP00000388324.2:n.-532+231del
ENST00000506622.5:c.908+231del	ENSP00000427249.1:n.908+231del
ENST00000509818.5:c.*16+231del	ENSP00000424085.1:n.*16+231del
ENST00000514561.5:c.*775+231del	ENSP00000422717.1:n.*775+231del
NM_014822.2:c.801+231del	NP_055637.2:n.801+231del
XM_005263378.1:c.804+231del	XP_005263435.1:n.804+231del
XM_005263379.1:c.804+231del	XP_005263436.1:n.804+231del
XM_011532435.1:c.804+231del	XP_011530737.1:n.804+231del
XM_011532436.1:c.804+231del	XP_011530738.1:n.804+231del
NM_001318066.1:c.804+231del	NP_001304995.1:n.804+231del
NM_014822.3:c.801+231del	NP_055637.2:n.801+231del
XM_005263379.3:c.804+231del	XP_005263436.1:n.804+231del
XM_024454293.1:c.801+231del	XP_024310061.1:n.801+231del
NM_014822.4:c.801+231del MANE Select	NP_055637.2:n.801+231del
NM_001318066.2:c.804+231del	NP_001304995.1:n.804+231del