Canonical Allele Identifier: CA3056884

Gene: SEC24D

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.118731451G>T , CM000666.2:g.118731451G>T	GRCh38
NC_000004.11:g.119652606G>T , CM000666.1:g.119652606G>T	GRCh37
NC_000004.10:g.119872054G>T	NCBI36
NG_042032.1:g.109721C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280551.11:c.2733C>A MANE Select	ENSP00000280551.6:p.Ser911=
ENST00000280551.10:c.2733C>A	ENSP00000280551.6:p.Ser911=
ENST00000505134.5:n.2864C>A
ENST00000511481.5:c.1626C>A	ENSP00000425491.1:p.Ser542=
ENST00000511715.1:n.640C>A
NM_014822.2:c.2733C>A	NP_055637.2:p.Ser911=
XM_005263378.1:c.2736C>A	XP_005263435.1:p.Ser912=
XM_005263379.1:c.2736C>A	XP_005263436.1:p.Ser912=
XM_011532435.1:c.2736C>A	XP_011530737.1:p.Ser912=
XM_011532437.1:c.1401C>A	XP_011530739.1:p.Ser467=
NM_001318066.1:c.2736C>A	NP_001304995.1:p.Ser912=
NM_014822.3:c.2733C>A	NP_055637.2:p.Ser911=
XM_005263379.3:c.2736C>A	XP_005263436.1:p.Ser912=
XM_017008875.1:c.1401C>A	XP_016864364.1:p.Ser467=
XM_024454293.1:c.2733C>A	XP_024310061.1:p.Ser911=
NM_014822.4:c.2733C>A MANE Select	NP_055637.2:p.Ser911=
NM_001318066.2:c.2736C>A	NP_001304995.1:p.Ser912=