Canonical Allele Identifier: CA2578175905

Gene: SEC24D

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.118739136G>A , CM000666.2:g.118739136G>A	GRCh38
NC_000004.11:g.119660291G>A , CM000666.1:g.119660291G>A	GRCh37
NC_000004.10:g.119879739G>A	NCBI36
NG_042032.1:g.102036C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_014822.4:c.2377+13C>T MANE Select	NP_055637.2:n.2377+13C>T
ENST00000280551.11:c.2377+13C>T MANE Select	ENSP00000280551.6:n.2377+13C>T
NM_001318066.1:c.2380+13C>T	NP_001304995.1:n.2380+13C>T
NM_001318066.2:c.2380+13C>T	NP_001304995.1:n.2380+13C>T
NM_014822.2:c.2377+13C>T	NP_055637.2:n.2377+13C>T
NM_014822.3:c.2377+13C>T	NP_055637.2:n.2377+13C>T
ENST00000280551.10:c.2377+13C>T	ENSP00000280551.6:n.2377+13C>T
ENST00000419654.6:c.1045+13C>T	ENSP00000388324.2:n.1045+13C>T
ENST00000502526.1:n.75+13C>T
ENST00000505134.5:n.1665+13C>T
ENST00000511481.5:c.1270+13C>T	ENSP00000425491.1:n.1270+13C>T
ENST00000514561.5:c.*2784+13C>T	ENSP00000422717.1:n.*2784+13C>T
XM_005263378.1:c.2380+13C>T	XP_005263435.1:n.2380+13C>T
XM_005263379.1:c.2380+13C>T	XP_005263436.1:n.2380+13C>T
XM_005263379.3:c.2380+13C>T	XP_005263436.1:n.2380+13C>T
XM_011532435.1:c.2380+13C>T	XP_011530737.1:n.2380+13C>T
XM_011532436.1:c.2380+13C>T	XP_011530738.1:n.2380+13C>T
XM_011532437.1:c.1045+13C>T	XP_011530739.1:n.1045+13C>T
XM_017008875.1:c.1045+13C>T	XP_016864364.1:n.1045+13C>T
XM_024454293.1:c.2377+13C>T	XP_024310061.1:n.2377+13C>T