Canonical Allele Identifier: CA441111082

Gene: SEC24D

Linked Data

• MyVariant Identifiers: chr4:g.119736670A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.118815515A>G , CM000666.2:g.118815515A>G	GRCh38
NC_000004.11:g.119736670A>G , CM000666.1:g.119736670A>G	GRCh37
NC_000004.10:g.119956118A>G	NCBI36
NG_042032.1:g.25657T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280551.11:c.609T>C MANE Select	ENSP00000280551.6:p.Asn203=
ENST00000280551.10:c.609T>C	ENSP00000280551.6:p.Asn203=
ENST00000419654.6:c.-724T>C	ENSP00000388324.2:n.-724T>C
ENST00000506622.5:c.716T>C	ENSP00000427249.1:p.Met239Thr
ENST00000509818.5:c.460T>C	ENSP00000424085.1:p.Cys154Arg
ENST00000514561.5:c.*583T>C	ENSP00000422717.1:n.*583T>C
NM_014822.2:c.609T>C	NP_055637.2:p.Asn203=
XM_005263378.1:c.609T>C	XP_005263435.1:p.Asn203=
XM_005263379.1:c.609T>C	XP_005263436.1:p.Asn203=
XM_011532435.1:c.609T>C	XP_011530737.1:p.Asn203=
XM_011532436.1:c.609T>C	XP_011530738.1:p.Asn203=
NM_001318066.1:c.609T>C	NP_001304995.1:p.Asn203=
NM_014822.3:c.609T>C	NP_055637.2:p.Asn203=
XM_005263379.3:c.609T>C	XP_005263436.1:p.Asn203=
XM_024454293.1:c.609T>C	XP_024310061.1:p.Asn203=
NM_014822.4:c.609T>C MANE Select	NP_055637.2:p.Asn203=
NM_001318066.2:c.609T>C	NP_001304995.1:p.Asn203=