Canonical Allele Identifier: CA1445208483

Gene: SEPSECS

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156738_25156746delinsAGTCTTTTC , CM000666.2:g.25156738_25156746delinsAGTCTTTTC	GRCh38
NC_000004.11:g.25158360_25158368delinsAGTCTTTTC , CM000666.1:g.25158360_25158368delinsAGTCTTTTC	GRCh37
NC_000004.10:g.24767458_24767466delinsAGTCTTTTC	NCBI36
NG_028222.1:g.8837_8845delinsGAAAAGACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.388+110_388+118delinsGAAAAGACT MANE Select	ENSP00000371535.2:n.388+110_388+118delinsGAAAAGACT
ENST00000680581.1:c.388+110_388+118delinsGAAAAGACT	ENSP00000506483.1:n.388+110_388+118delinsGAAAAGACT
ENST00000680824.1:n.1604+110_1604+118delinsGAAAAGACT
ENST00000681071.1:n.680+110_680+118delinsGAAAAGACT
ENST00000681166.1:n.1435+110_1435+118delinsGAAAAGACT
ENST00000681341.1:n.1529+110_1529+118delinsGAAAAGACT
ENST00000681640.1:n.482+110_482+118delinsGAAAAGACT
ENST00000681948.1:c.643+110_643+118delinsGAAAAGACT	ENSP00000505991.1:n.643+110_643+118delinsGAAAAGACT
ENST00000358971.7:c.*186+110_*186+118delinsGAAAAGACT	ENSP00000351857.3:n.*186+110_*186+118delinsGAAAAGACT
ENST00000382103.6:c.388+110_388+118delinsGAAAAGACT	ENSP00000371535.2:n.388+110_388+118delinsGAAAAGACT
ENST00000514585.5:c.*89+110_*89+118delinsGAAAAGACT	ENSP00000421880.1:n.*89+110_*89+118delinsGAAAAGACT
NM_016955.3:c.388+110_388+118delinsGAAAAGACT	NP_058651.3:n.388+110_388+118delinsGAAAAGACT
XM_005248168.2:c.151+110_151+118delinsGAAAAGACT	XP_005248225.1:n.151+110_151+118delinsGAAAAGACT
XM_006713965.2:c.208+110_208+118delinsGAAAAGACT	XP_006714028.1:n.208+110_208+118delinsGAAAAGACT
XM_011513846.1:c.385+110_385+118delinsGAAAAGACT	XP_011512148.1:n.385+110_385+118delinsGAAAAGACT
XM_011513847.1:c.355+110_355+118delinsGAAAAGACT	XP_011512149.1:n.355+110_355+118delinsGAAAAGACT
XM_011513848.1:c.208+110_208+118delinsGAAAAGACT	XP_011512150.1:n.208+110_208+118delinsGAAAAGACT
XM_011513846.2:c.385+110_385+118delinsGAAAAGACT	XP_011512148.1:n.385+110_385+118delinsGAAAAGACT
XM_011513847.2:c.355+110_355+118delinsGAAAAGACT	XP_011512149.1:n.355+110_355+118delinsGAAAAGACT
XM_017008277.1:c.643+110_643+118delinsGAAAAGACT	XP_016863766.1:n.643+110_643+118delinsGAAAAGACT
XM_017008278.1:c.-36+110_-36+118delinsGAAAAGACT	XP_016863767.1:n.-36+110_-36+118delinsGAAAAGACT
NM_016955.4:c.388+110_388+118delinsGAAAAGACT MANE Select	NP_058651.3:n.388+110_388+118delinsGAAAAGACT