Canonical Allele Identifier: CA2670220969

Gene: SEPSECS

Linked Data

• gnomAD v4: 4-25120652-A-AGCT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25120653_25120654insCTG , CM000666.2:g.25120653_25120654insCTG	GRCh38
NC_000004.11:g.25122275_25122276insCTG , CM000666.1:g.25122275_25122276insCTG	GRCh37
NC_000004.10:g.24731373_24731374insCTG	NCBI36
NG_028222.1:g.44930_44931insAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.*3278_*3279insAGC MANE Select	ENSP00000371535.2:n.*3278_*3279insAGC
ENST00000680581.1:c.*3658_*3659insAGC	ENSP00000506483.1:n.*3658_*3659insAGC
ENST00000680824.1:n.6000_6001insAGC
ENST00000681071.1:n.5076_5077insAGC
ENST00000681341.1:n.5831_5832insAGC
ENST00000681374.1:n.4140_4141insAGC
ENST00000681948.1:c.*3278_*3279insAGC	ENSP00000505991.1:n.*3278_*3279insAGC
ENST00000382103.6:c.*3278_*3279insAGC	ENSP00000371535.2:n.*3278_*3279insAGC
NM_016955.3:c.*3278_*3279insAGC	NP_058651.3:n.*3278_*3279insAGC
XM_005248168.2:c.*3278_*3279insAGC	XP_005248225.1:n.*3278_*3279insAGC
XM_006713965.2:c.*3278_*3279insAGC	XP_006714028.1:n.*3278_*3279insAGC
XM_011513846.1:c.*3278_*3279insAGC	XP_011512148.1:n.*3278_*3279insAGC
XM_011513847.1:c.*3278_*3279insAGC	XP_011512149.1:n.*3278_*3279insAGC
XM_011513848.1:c.*3278_*3279insAGC	XP_011512150.1:n.*3278_*3279insAGC
XM_011513846.2:c.*3278_*3279insAGC	XP_011512148.1:n.*3278_*3279insAGC
XM_011513847.2:c.*3278_*3279insAGC	XP_011512149.1:n.*3278_*3279insAGC
XM_017008277.1:c.*3278_*3279insAGC	XP_016863766.1:n.*3278_*3279insAGC
XM_017008278.1:c.*3278_*3279insAGC	XP_016863767.1:n.*3278_*3279insAGC
NM_016955.4:c.*3278_*3279insAGC MANE Select	NP_058651.3:n.*3278_*3279insAGC