Canonical Allele Identifier: CA441111098

Gene: SEC24D

Linked Data

• MyVariant Identifiers: chr4:g.119736679A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.118815524A>C , CM000666.2:g.118815524A>C	GRCh38
NC_000004.11:g.119736679A>C , CM000666.1:g.119736679A>C	GRCh37
NC_000004.10:g.119956127A>C	NCBI36
NG_042032.1:g.25648T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280551.11:c.600T>G MANE Select	ENSP00000280551.6:p.Pro200=
ENST00000280551.10:c.600T>G	ENSP00000280551.6:p.Pro200=
ENST00000419654.6:c.-733T>G	ENSP00000388324.2:n.-733T>G
ENST00000506622.5:c.707T>G	ENSP00000427249.1:p.Leu236Arg
ENST00000509818.5:c.451T>G	ENSP00000424085.1:p.Ser151Ala
ENST00000514561.5:c.*574T>G	ENSP00000422717.1:n.*574T>G
NM_014822.2:c.600T>G	NP_055637.2:p.Pro200=
XM_005263378.1:c.600T>G	XP_005263435.1:p.Pro200=
XM_005263379.1:c.600T>G	XP_005263436.1:p.Pro200=
XM_011532435.1:c.600T>G	XP_011530737.1:p.Pro200=
XM_011532436.1:c.600T>G	XP_011530738.1:p.Pro200=
NM_001318066.1:c.600T>G	NP_001304995.1:p.Pro200=
NM_014822.3:c.600T>G	NP_055637.2:p.Pro200=
XM_005263379.3:c.600T>G	XP_005263436.1:p.Pro200=
XM_024454293.1:c.600T>G	XP_024310061.1:p.Pro200=
NM_014822.4:c.600T>G MANE Select	NP_055637.2:p.Pro200=
NM_001318066.2:c.600T>G	NP_001304995.1:p.Pro200=