Canonical Allele Identifier: CA1488655423

Gene: SEC24D

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.118815518_118815521delinsTGGA , CM000666.2:g.118815518_118815521delinsTGGA	GRCh38
NC_000004.11:g.119736673_119736676delinsTGGA , CM000666.1:g.119736673_119736676delinsTGGA	GRCh37
NC_000004.10:g.119956121_119956124delinsTGGA	NCBI36
NG_042032.1:g.25651_25654delinsTCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280551.11:c.603_606delinsTCCA MANE Select	ENSP00000280551.6:p.Pro201=
ENST00000280551.10:c.603_606delinsTCCA	ENSP00000280551.6:p.Pro201=
ENST00000419654.6:c.-730_-727delinsTCCA	ENSP00000388324.2:n.-730_-727delinsTCCA
ENST00000506622.5:c.710_713delinsTCCA	ENSP00000427249.1:p.Leu237=
ENST00000509818.5:c.454_457delinsTCCA	ENSP00000424085.1:p.Ser152=
ENST00000514561.5:c.*577_*580delinsTCCA	ENSP00000422717.1:n.*577_*580delinsTCCA
NM_014822.2:c.603_606delinsTCCA	NP_055637.2:p.Pro201=
XM_005263378.1:c.603_606delinsTCCA	XP_005263435.1:p.Pro201=
XM_005263379.1:c.603_606delinsTCCA	XP_005263436.1:p.Pro201=
XM_011532435.1:c.603_606delinsTCCA	XP_011530737.1:p.Pro201=
XM_011532436.1:c.603_606delinsTCCA	XP_011530738.1:p.Pro201=
NM_001318066.1:c.603_606delinsTCCA	NP_001304995.1:p.Pro201=
NM_014822.3:c.603_606delinsTCCA	NP_055637.2:p.Pro201=
XM_005263379.3:c.603_606delinsTCCA	XP_005263436.1:p.Pro201=
XM_024454293.1:c.603_606delinsTCCA	XP_024310061.1:p.Pro201=
NM_014822.4:c.603_606delinsTCCA MANE Select	NP_055637.2:p.Pro201=
NM_001318066.2:c.603_606delinsTCCA	NP_001304995.1:p.Pro201=