Canonical Allele Identifier: CA1488655424

Gene: SEC24D

Linked Data

• dbSNP Id: rs1730105655
• gnomAD v4: 4-118815518-TGGA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.118815527_118815529del , CM000666.2:g.118815527_118815529del	GRCh38
NC_000004.11:g.119736682_119736684del , CM000666.1:g.119736682_119736684del	GRCh37
NC_000004.10:g.119956130_119956132del	NCBI36
NG_042032.1:g.25651_25653del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280551.11:c.603_605del MANE Select	ENSP00000280551.6:p.Pro202del
ENST00000280551.10:c.603_605del	ENSP00000280551.6:p.Pro202del
ENST00000419654.6:c.-730_-728del	ENSP00000388324.2:n.-730_-728del
ENST00000506622.5:c.710_712del	ENSP00000427249.1:p.Leu237del
ENST00000509818.5:c.454_456del	ENSP00000424085.1:p.Ser152del
ENST00000514561.5:c.*577_*579del	ENSP00000422717.1:n.*577_*579del
NM_014822.2:c.603_605del	NP_055637.2:p.Pro202del
XM_005263378.1:c.603_605del	XP_005263435.1:p.Pro202del
XM_005263379.1:c.603_605del	XP_005263436.1:p.Pro202del
XM_011532435.1:c.603_605del	XP_011530737.1:p.Pro202del
XM_011532436.1:c.603_605del	XP_011530738.1:p.Pro202del
NM_001318066.1:c.603_605del	NP_001304995.1:p.Pro202del
NM_014822.3:c.603_605del	NP_055637.2:p.Pro202del
XM_005263379.3:c.603_605del	XP_005263436.1:p.Pro202del
XM_024454293.1:c.603_605del	XP_024310061.1:p.Pro202del
NM_014822.4:c.603_605del MANE Select	NP_055637.2:p.Pro202del
NM_001318066.2:c.603_605del	NP_001304995.1:p.Pro202del