Canonical Allele Identifier: CA2670197163

Gene: SEPSECS

Linked Data

• gnomAD v4: 4-25156733-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156733_25156734insG , CM000666.2:g.25156733_25156734insG	GRCh38
NC_000004.11:g.25158355_25158356insG , CM000666.1:g.25158355_25158356insG	GRCh37
NC_000004.10:g.24767453_24767454insG	NCBI36
NG_028222.1:g.8849_8850insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.388+122_388+123insC MANE Select	ENSP00000371535.2:n.388+122_388+123insC
ENST00000680581.1:c.388+122_388+123insC	ENSP00000506483.1:n.388+122_388+123insC
ENST00000680824.1:n.1604+122_1604+123insC
ENST00000681071.1:n.680+122_680+123insC
ENST00000681166.1:n.1435+122_1435+123insC
ENST00000681341.1:n.1529+122_1529+123insC
ENST00000681640.1:n.482+122_482+123insC
ENST00000681948.1:c.643+122_643+123insC	ENSP00000505991.1:n.643+122_643+123insC
ENST00000358971.7:c.*186+122_*186+123insC	ENSP00000351857.3:n.*186+122_*186+123insC
ENST00000382103.6:c.388+122_388+123insC	ENSP00000371535.2:n.388+122_388+123insC
ENST00000514585.5:c.*89+122_*89+123insC	ENSP00000421880.1:n.*89+122_*89+123insC
NM_016955.3:c.388+122_388+123insC	NP_058651.3:n.388+122_388+123insC
XM_005248168.2:c.151+122_151+123insC	XP_005248225.1:n.151+122_151+123insC
XM_006713965.2:c.208+122_208+123insC	XP_006714028.1:n.208+122_208+123insC
XM_011513846.1:c.385+122_385+123insC	XP_011512148.1:n.385+122_385+123insC
XM_011513847.1:c.355+122_355+123insC	XP_011512149.1:n.355+122_355+123insC
XM_011513848.1:c.208+122_208+123insC	XP_011512150.1:n.208+122_208+123insC
XM_011513846.2:c.385+122_385+123insC	XP_011512148.1:n.385+122_385+123insC
XM_011513847.2:c.355+122_355+123insC	XP_011512149.1:n.355+122_355+123insC
XM_017008277.1:c.643+122_643+123insC	XP_016863766.1:n.643+122_643+123insC
XM_017008278.1:c.-36+122_-36+123insC	XP_016863767.1:n.-36+122_-36+123insC
NM_016955.4:c.388+122_388+123insC MANE Select	NP_058651.3:n.388+122_388+123insC