Canonical Allele Identifier: CA2760775112

Gene: SEPSECS

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156734_25156735insT , CM000666.2:g.25156734_25156735insT	GRCh38
NC_000004.11:g.25158356_25158357insT , CM000666.1:g.25158356_25158357insT	GRCh37
NC_000004.10:g.24767454_24767455insT	NCBI36
NG_028222.1:g.8848_8849insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.388+121_388+122insA MANE Select	ENSP00000371535.2:n.388+121_388+122insA
ENST00000680581.1:c.388+121_388+122insA	ENSP00000506483.1:n.388+121_388+122insA
ENST00000680824.1:n.1604+121_1604+122insA
ENST00000681071.1:n.680+121_680+122insA
ENST00000681166.1:n.1435+121_1435+122insA
ENST00000681341.1:n.1529+121_1529+122insA
ENST00000681640.1:n.482+121_482+122insA
ENST00000681948.1:c.643+121_643+122insA	ENSP00000505991.1:n.643+121_643+122insA
ENST00000358971.7:c.*186+121_*186+122insA	ENSP00000351857.3:n.*186+121_*186+122insA
ENST00000382103.6:c.388+121_388+122insA	ENSP00000371535.2:n.388+121_388+122insA
ENST00000514585.5:c.*89+121_*89+122insA	ENSP00000421880.1:n.*89+121_*89+122insA
NM_016955.3:c.388+121_388+122insA	NP_058651.3:n.388+121_388+122insA
XM_005248168.2:c.151+121_151+122insA	XP_005248225.1:n.151+121_151+122insA
XM_006713965.2:c.208+121_208+122insA	XP_006714028.1:n.208+121_208+122insA
XM_011513846.1:c.385+121_385+122insA	XP_011512148.1:n.385+121_385+122insA
XM_011513847.1:c.355+121_355+122insA	XP_011512149.1:n.355+121_355+122insA
XM_011513848.1:c.208+121_208+122insA	XP_011512150.1:n.208+121_208+122insA
XM_011513846.2:c.385+121_385+122insA	XP_011512148.1:n.385+121_385+122insA
XM_011513847.2:c.355+121_355+122insA	XP_011512149.1:n.355+121_355+122insA
XM_017008277.1:c.643+121_643+122insA	XP_016863766.1:n.643+121_643+122insA
XM_017008278.1:c.-36+121_-36+122insA	XP_016863767.1:n.-36+121_-36+122insA
NM_016955.4:c.388+121_388+122insA MANE Select	NP_058651.3:n.388+121_388+122insA