Canonical Allele Identifier: CA2502657761

Gene: SEPSECS

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156723_25156724insG , CM000666.2:g.25156723_25156724insG	GRCh38
NC_000004.11:g.25158345_25158346insG , CM000666.1:g.25158345_25158346insG	GRCh37
NC_000004.10:g.24767443_24767444insG	NCBI36
NG_028222.1:g.8859_8860insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.388+132_388+133insC MANE Select	ENSP00000371535.2:n.388+132_388+133insC
ENST00000680581.1:c.388+132_388+133insC	ENSP00000506483.1:n.388+132_388+133insC
ENST00000680824.1:n.1604+132_1604+133insC
ENST00000681071.1:n.680+132_680+133insC
ENST00000681166.1:n.1435+132_1435+133insC
ENST00000681341.1:n.1529+132_1529+133insC
ENST00000681640.1:n.482+132_482+133insC
ENST00000681948.1:c.643+132_643+133insC	ENSP00000505991.1:n.643+132_643+133insC
ENST00000358971.7:c.*186+132_*186+133insC	ENSP00000351857.3:n.*186+132_*186+133insC
ENST00000382103.6:c.388+132_388+133insC	ENSP00000371535.2:n.388+132_388+133insC
ENST00000514585.5:c.*89+132_*89+133insC	ENSP00000421880.1:n.*89+132_*89+133insC
NM_016955.3:c.388+132_388+133insC	NP_058651.3:n.388+132_388+133insC
XM_005248168.2:c.151+132_151+133insC	XP_005248225.1:n.151+132_151+133insC
XM_006713965.2:c.208+132_208+133insC	XP_006714028.1:n.208+132_208+133insC
XM_011513846.1:c.385+132_385+133insC	XP_011512148.1:n.385+132_385+133insC
XM_011513847.1:c.355+132_355+133insC	XP_011512149.1:n.355+132_355+133insC
XM_011513848.1:c.208+132_208+133insC	XP_011512150.1:n.208+132_208+133insC
XM_011513846.2:c.385+132_385+133insC	XP_011512148.1:n.385+132_385+133insC
XM_011513847.2:c.355+132_355+133insC	XP_011512149.1:n.355+132_355+133insC
XM_017008277.1:c.643+132_643+133insC	XP_016863766.1:n.643+132_643+133insC
XM_017008278.1:c.-36+132_-36+133insC	XP_016863767.1:n.-36+132_-36+133insC
NM_016955.4:c.388+132_388+133insC MANE Select	NP_058651.3:n.388+132_388+133insC