Canonical Allele Identifier: CA1445208583

Gene: SEPSECS

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156802_25156804delinsGGT , CM000666.2:g.25156802_25156804delinsGGT	GRCh38
NC_000004.11:g.25158424_25158426delinsGGT , CM000666.1:g.25158424_25158426delinsGGT	GRCh37
NC_000004.10:g.24767522_24767524delinsGGT	NCBI36
NG_028222.1:g.8779_8781delinsACC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.388+52_388+54delinsACC MANE Select	ENSP00000371535.2:n.388+52_388+54delinsACC
ENST00000680581.1:c.388+52_388+54delinsACC	ENSP00000506483.1:n.388+52_388+54delinsACC
ENST00000680824.1:n.1604+52_1604+54delinsACC
ENST00000681071.1:n.680+52_680+54delinsACC
ENST00000681166.1:n.1435+52_1435+54delinsACC
ENST00000681341.1:n.1529+52_1529+54delinsACC
ENST00000681640.1:n.482+52_482+54delinsACC
ENST00000681948.1:c.643+52_643+54delinsACC	ENSP00000505991.1:n.643+52_643+54delinsACC
ENST00000358971.7:c.*186+52_*186+54delinsACC	ENSP00000351857.3:n.*186+52_*186+54delinsACC
ENST00000382103.6:c.388+52_388+54delinsACC	ENSP00000371535.2:n.388+52_388+54delinsACC
ENST00000514585.5:c.*89+52_*89+54delinsACC	ENSP00000421880.1:n.*89+52_*89+54delinsACC
NM_016955.3:c.388+52_388+54delinsACC	NP_058651.3:n.388+52_388+54delinsACC
XM_005248168.2:c.151+52_151+54delinsACC	XP_005248225.1:n.151+52_151+54delinsACC
XM_006713965.2:c.208+52_208+54delinsACC	XP_006714028.1:n.208+52_208+54delinsACC
XM_011513846.1:c.385+52_385+54delinsACC	XP_011512148.1:n.385+52_385+54delinsACC
XM_011513847.1:c.355+52_355+54delinsACC	XP_011512149.1:n.355+52_355+54delinsACC
XM_011513848.1:c.208+52_208+54delinsACC	XP_011512150.1:n.208+52_208+54delinsACC
XM_011513846.2:c.385+52_385+54delinsACC	XP_011512148.1:n.385+52_385+54delinsACC
XM_011513847.2:c.355+52_355+54delinsACC	XP_011512149.1:n.355+52_355+54delinsACC
XM_017008277.1:c.643+52_643+54delinsACC	XP_016863766.1:n.643+52_643+54delinsACC
XM_017008278.1:c.-36+52_-36+54delinsACC	XP_016863767.1:n.-36+52_-36+54delinsACC
NM_016955.4:c.388+52_388+54delinsACC MANE Select	NP_058651.3:n.388+52_388+54delinsACC