Canonical Allele Identifier: CA554159738

Gene: SEC24D

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.118739130A>G , CM000666.2:g.118739130A>G	GRCh38
NC_000004.11:g.119660285A>G , CM000666.1:g.119660285A>G	GRCh37
NC_000004.10:g.119879733A>G	NCBI36
NG_042032.1:g.102042T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_014822.4:c.2377+19T>C MANE Select	NP_055637.2:n.2377+19T>C
ENST00000280551.11:c.2377+19T>C MANE Select	ENSP00000280551.6:n.2377+19T>C
NM_001318066.1:c.2380+19T>C	NP_001304995.1:n.2380+19T>C
NM_001318066.2:c.2380+19T>C	NP_001304995.1:n.2380+19T>C
NM_014822.2:c.2377+19T>C	NP_055637.2:n.2377+19T>C
NM_014822.3:c.2377+19T>C	NP_055637.2:n.2377+19T>C
ENST00000280551.10:c.2377+19T>C	ENSP00000280551.6:n.2377+19T>C
ENST00000419654.6:c.1045+19T>C	ENSP00000388324.2:n.1045+19T>C
ENST00000502526.1:n.75+19T>C
ENST00000505134.5:n.1665+19T>C
ENST00000511481.5:c.1270+19T>C	ENSP00000425491.1:n.1270+19T>C
ENST00000514561.5:c.*2784+19T>C	ENSP00000422717.1:n.*2784+19T>C
XM_005263378.1:c.2380+19T>C	XP_005263435.1:n.2380+19T>C
XM_005263379.1:c.2380+19T>C	XP_005263436.1:n.2380+19T>C
XM_005263379.3:c.2380+19T>C	XP_005263436.1:n.2380+19T>C
XM_011532435.1:c.2380+19T>C	XP_011530737.1:n.2380+19T>C
XM_011532436.1:c.2380+19T>C	XP_011530738.1:n.2380+19T>C
XM_011532437.1:c.1045+19T>C	XP_011530739.1:n.1045+19T>C
XM_017008875.1:c.1045+19T>C	XP_016864364.1:n.1045+19T>C
XM_024454293.1:c.2377+19T>C	XP_024310061.1:n.2377+19T>C