Canonical Allele Identifier: CA1445208183

Gene: SEPSECS

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156687_25156689delinsAAC , CM000666.2:g.25156687_25156689delinsAAC	GRCh38
NC_000004.11:g.25158309_25158311delinsAAC , CM000666.1:g.25158309_25158311delinsAAC	GRCh37
NC_000004.10:g.24767407_24767409delinsAAC	NCBI36
NG_028222.1:g.8894_8896delinsGTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000382103.7:c.388+167_388+169delinsGTT MANE Select	ENSP00000371535.2:n.388+167_388+169delins...
ENST00000680581.1:c.388+167_388+169delinsGTT	ENSP00000506483.1:n.388+167_388+169delins...
ENST00000680824.1:n.1604+167_1604+169delinsGTT
ENST00000681071.1:n.680+167_680+169delinsGTT
ENST00000681166.1:n.1435+167_1435+169delinsGTT
ENST00000681341.1:n.1529+167_1529+169delinsGTT
ENST00000681640.1:n.482+167_482+169delinsGTT
ENST00000681948.1:c.643+167_643+169delinsGTT	ENSP00000505991.1:n.643+167_643+169delins...
ENST00000358971.7:c.*186+167_*186+169delinsGTT	ENSP00000351857.3:n.*186+167_*186+169deli...
ENST00000382103.6:c.388+167_388+169delinsGTT	ENSP00000371535.2:n.388+167_388+169delins...
ENST00000514585.5:c.*89+167_*89+169delinsGTT	ENSP00000421880.1:n.*89+167_*89+169delins...
NM_016955.3:c.388+167_388+169delinsGTT	NP_058651.3:n.388+167_388+169delinsGTT
XM_005248168.2:c.151+167_151+169delinsGTT	XP_005248225.1:n.151+167_151+169delinsGTT...
XM_006713965.2:c.208+167_208+169delinsGTT	XP_006714028.1:n.208+167_208+169delinsGTT...
XM_011513846.1:c.385+167_385+169delinsGTT	XP_011512148.1:n.385+167_385+169delinsGTT...
XM_011513847.1:c.355+167_355+169delinsGTT	XP_011512149.1:n.355+167_355+169delinsGTT...
XM_011513848.1:c.208+167_208+169delinsGTT	XP_011512150.1:n.208+167_208+169delinsGTT...
XM_011513846.2:c.385+167_385+169delinsGTT	XP_011512148.1:n.385+167_385+169delinsGTT...
XM_011513847.2:c.355+167_355+169delinsGTT	XP_011512149.1:n.355+167_355+169delinsGTT...
XM_017008277.1:c.643+167_643+169delinsGTT	XP_016863766.1:n.643+167_643+169delinsGTT...
XM_017008278.1:c.-36+167_-36+169delinsGTT	XP_016863767.1:n.-36+167_-36+169delinsGTT...
NM_016955.4:c.388+167_388+169delinsGTT MANE Select	NP_058651.3:n.388+167_388+169delinsGTT