Canonical Allele Identifier: CA3056897

Gene: SEC24D

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.118731528G>C , CM000666.2:g.118731528G>C	GRCh38
NC_000004.11:g.119652683G>C , CM000666.1:g.119652683G>C	GRCh37
NC_000004.10:g.119872131G>C	NCBI36
NG_042032.1:g.109644C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280551.11:c.2677-21C>G MANE Select	ENSP00000280551.6:n.2677-21C>G
ENST00000280551.10:c.2677-21C>G	ENSP00000280551.6:n.2677-21C>G
ENST00000505134.5:n.2808-21C>G
ENST00000511481.5:c.1570-21C>G	ENSP00000425491.1:n.1570-21C>G
ENST00000511715.1:n.584-21C>G
NM_014822.2:c.2677-21C>G	NP_055637.2:n.2677-21C>G
XM_005263378.1:c.2680-21C>G	XP_005263435.1:n.2680-21C>G
XM_005263379.1:c.2680-21C>G	XP_005263436.1:n.2680-21C>G
XM_011532435.1:c.2680-21C>G	XP_011530737.1:n.2680-21C>G
XM_011532437.1:c.1345-21C>G	XP_011530739.1:n.1345-21C>G
NM_001318066.1:c.2680-21C>G	NP_001304995.1:n.2680-21C>G
NM_014822.3:c.2677-21C>G	NP_055637.2:n.2677-21C>G
XM_005263379.3:c.2680-21C>G	XP_005263436.1:n.2680-21C>G
XM_017008875.1:c.1345-21C>G	XP_016864364.1:n.1345-21C>G
XM_024454293.1:c.2677-21C>G	XP_024310061.1:n.2677-21C>G
NM_014822.4:c.2677-21C>G MANE Select	NP_055637.2:n.2677-21C>G
NM_001318066.2:c.2680-21C>G	NP_001304995.1:n.2680-21C>G