Canonical Allele Identifier: CA2705079586

Gene: SEPSECS

Linked Data

• dbSNP Id: rs1712670901

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156706_25156707insAA , CM000666.2:g.25156706_25156707insAA	GRCh38
NC_000004.11:g.25158328_25158329insAA , CM000666.1:g.25158328_25158329insAA	GRCh37
NC_000004.10:g.24767426_24767427insAA	NCBI36
NG_028222.1:g.8876_8877insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.388+149_388+150insTT MANE Select	ENSP00000371535.2:n.388+149_388+150insTT
ENST00000680581.1:c.388+149_388+150insTT	ENSP00000506483.1:n.388+149_388+150insTT
ENST00000680824.1:n.1604+149_1604+150insTT
ENST00000681071.1:n.680+149_680+150insTT
ENST00000681166.1:n.1435+149_1435+150insTT
ENST00000681341.1:n.1529+149_1529+150insTT
ENST00000681640.1:n.482+149_482+150insTT
ENST00000681948.1:c.643+149_643+150insTT	ENSP00000505991.1:n.643+149_643+150insTT
ENST00000358971.7:c.*186+149_*186+150insTT	ENSP00000351857.3:n.*186+149_*186+150insTT
ENST00000382103.6:c.388+149_388+150insTT	ENSP00000371535.2:n.388+149_388+150insTT
ENST00000514585.5:c.*89+149_*89+150insTT	ENSP00000421880.1:n.*89+149_*89+150insTT
NM_016955.3:c.388+149_388+150insTT	NP_058651.3:n.388+149_388+150insTT
XM_005248168.2:c.151+149_151+150insTT	XP_005248225.1:n.151+149_151+150insTT
XM_006713965.2:c.208+149_208+150insTT	XP_006714028.1:n.208+149_208+150insTT
XM_011513846.1:c.385+149_385+150insTT	XP_011512148.1:n.385+149_385+150insTT
XM_011513847.1:c.355+149_355+150insTT	XP_011512149.1:n.355+149_355+150insTT
XM_011513848.1:c.208+149_208+150insTT	XP_011512150.1:n.208+149_208+150insTT
XM_011513846.2:c.385+149_385+150insTT	XP_011512148.1:n.385+149_385+150insTT
XM_011513847.2:c.355+149_355+150insTT	XP_011512149.1:n.355+149_355+150insTT
XM_017008277.1:c.643+149_643+150insTT	XP_016863766.1:n.643+149_643+150insTT
XM_017008278.1:c.-36+149_-36+150insTT	XP_016863767.1:n.-36+149_-36+150insTT
NM_016955.4:c.388+149_388+150insTT MANE Select	NP_058651.3:n.388+149_388+150insTT