Canonical Allele Identifier: CA2760775102

Gene: SEPSECS

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156732_25156733insG , CM000666.2:g.25156732_25156733insG	GRCh38
NC_000004.11:g.25158354_25158355insG , CM000666.1:g.25158354_25158355insG	GRCh37
NC_000004.10:g.24767452_24767453insG	NCBI36
NG_028222.1:g.8850_8851insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.388+123_388+124insC MANE Select	ENSP00000371535.2:n.388+123_388+124insC
ENST00000680581.1:c.388+123_388+124insC	ENSP00000506483.1:n.388+123_388+124insC
ENST00000680824.1:n.1604+123_1604+124insC
ENST00000681071.1:n.680+123_680+124insC
ENST00000681166.1:n.1435+123_1435+124insC
ENST00000681341.1:n.1529+123_1529+124insC
ENST00000681640.1:n.482+123_482+124insC
ENST00000681948.1:c.643+123_643+124insC	ENSP00000505991.1:n.643+123_643+124insC
ENST00000358971.7:c.*186+123_*186+124insC	ENSP00000351857.3:n.*186+123_*186+124insC
ENST00000382103.6:c.388+123_388+124insC	ENSP00000371535.2:n.388+123_388+124insC
ENST00000514585.5:c.*89+123_*89+124insC	ENSP00000421880.1:n.*89+123_*89+124insC
NM_016955.3:c.388+123_388+124insC	NP_058651.3:n.388+123_388+124insC
XM_005248168.2:c.151+123_151+124insC	XP_005248225.1:n.151+123_151+124insC
XM_006713965.2:c.208+123_208+124insC	XP_006714028.1:n.208+123_208+124insC
XM_011513846.1:c.385+123_385+124insC	XP_011512148.1:n.385+123_385+124insC
XM_011513847.1:c.355+123_355+124insC	XP_011512149.1:n.355+123_355+124insC
XM_011513848.1:c.208+123_208+124insC	XP_011512150.1:n.208+123_208+124insC
XM_011513846.2:c.385+123_385+124insC	XP_011512148.1:n.385+123_385+124insC
XM_011513847.2:c.355+123_355+124insC	XP_011512149.1:n.355+123_355+124insC
XM_017008277.1:c.643+123_643+124insC	XP_016863766.1:n.643+123_643+124insC
XM_017008278.1:c.-36+123_-36+124insC	XP_016863767.1:n.-36+123_-36+124insC
NM_016955.4:c.388+123_388+124insC MANE Select	NP_058651.3:n.388+123_388+124insC