Canonical Allele Identifier: CA11894349

Gene: SEC24D

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.118745310T>A , CM000666.2:g.118745310T>A	GRCh38
NC_000004.11:g.119666465T>A , CM000666.1:g.119666465T>A	GRCh37
NC_000004.10:g.119885913T>A	NCBI36
NG_042032.1:g.95862A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000280551.11:c.1708-250A>T MANE Select	ENSP00000280551.6:n.1708-250A>T
ENST00000280551.10:c.1708-250A>T	ENSP00000280551.6:n.1708-250A>T
ENST00000419654.6:c.376-250A>T	ENSP00000388324.2:n.376-250A>T
ENST00000505134.5:n.996-250A>T
ENST00000511033.1:n.375-250A>T
ENST00000511481.5:c.601-250A>T	ENSP00000425491.1:n.601-250A>T
ENST00000514561.5:c.*2115-250A>T	ENSP00000422717.1:n.*2115-250A>T
NM_014822.2:c.1708-250A>T	NP_055637.2:n.1708-250A>T
XM_005263378.1:c.1711-250A>T	XP_005263435.1:n.1711-250A>T
XM_005263379.1:c.1711-250A>T	XP_005263436.1:n.1711-250A>T
XM_011532435.1:c.1711-250A>T	XP_011530737.1:n.1711-250A>T
XM_011532436.1:c.1711-250A>T	XP_011530738.1:n.1711-250A>T
XM_011532437.1:c.376-250A>T	XP_011530739.1:n.376-250A>T
NM_001318066.1:c.1711-250A>T	NP_001304995.1:n.1711-250A>T
NM_014822.3:c.1708-250A>T	NP_055637.2:n.1708-250A>T
XM_005263379.3:c.1711-250A>T	XP_005263436.1:n.1711-250A>T
XM_017008875.1:c.376-250A>T	XP_016864364.1:n.376-250A>T
XM_024454293.1:c.1708-250A>T	XP_024310061.1:n.1708-250A>T
NM_014822.4:c.1708-250A>T MANE Select	NP_055637.2:n.1708-250A>T
NM_001318066.2:c.1711-250A>T	NP_001304995.1:n.1711-250A>T