Canonical Allele Identifier: CA1445208239

Gene: SEPSECS

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156706_25156717delinsTCAAAAAAAAAA , CM000666.2:g.25156706_25156717delinsTCAAAAAAAAAA	GRCh38
NC_000004.11:g.25158328_25158339delinsTCAAAAAAAAAA , CM000666.1:g.25158328_25158339delinsTCAAAAAAAAAA	GRCh37
NC_000004.10:g.24767426_24767437delinsTCAAAAAAAAAA	NCBI36
NG_028222.1:g.8866_8877delinsTTTTTTTTTTGA

Transcript Alleles

HGVS	Amino-acid change
ENST00000382103.7:c.388+139_388+150delinsTTTTTTTTTTGA MANE Select	ENSP00000371535.2:n.388+139_388+150delinsTTTTTTTTTTGA
ENST00000680581.1:c.388+139_388+150delinsTTTTTTTTTTGA	ENSP00000506483.1:n.388+139_388+150delinsTTTTTTTTTTGA
ENST00000680824.1:n.1604+139_1604+150delinsTTTTTTTTTTGA
ENST00000681071.1:n.680+139_680+150delinsTTTTTTTTTTGA
ENST00000681166.1:n.1435+139_1435+150delinsTTTTTTTTTTGA
ENST00000681341.1:n.1529+139_1529+150delinsTTTTTTTTTTGA
ENST00000681640.1:n.482+139_482+150delinsTTTTTTTTTTGA
ENST00000681948.1:c.643+139_643+150delinsTTTTTTTTTTGA	ENSP00000505991.1:n.643+139_643+150delinsTTTTTTTTTTGA
ENST00000358971.7:c.*186+139_*186+150delinsTTTTTTTTTTGA	ENSP00000351857.3:n.*186+139_*186+150delinsTTTTTTTTTTGA
ENST00000382103.6:c.388+139_388+150delinsTTTTTTTTTTGA	ENSP00000371535.2:n.388+139_388+150delinsTTTTTTTTTTGA
ENST00000514585.5:c.*89+139_*89+150delinsTTTTTTTTTTGA	ENSP00000421880.1:n.*89+139_*89+150delinsTTTTTTTTTTGA
NM_016955.3:c.388+139_388+150delinsTTTTTTTTTTGA	NP_058651.3:n.388+139_388+150delinsTTTTTTTTTTGA
XM_005248168.2:c.151+139_151+150delinsTTTTTTTTTTGA	XP_005248225.1:n.151+139_151+150delinsTTTTTTTTTTGA
XM_006713965.2:c.208+139_208+150delinsTTTTTTTTTTGA	XP_006714028.1:n.208+139_208+150delinsTTTTTTTTTTGA
XM_011513846.1:c.385+139_385+150delinsTTTTTTTTTTGA	XP_011512148.1:n.385+139_385+150delinsTTTTTTTTTTGA
XM_011513847.1:c.355+139_355+150delinsTTTTTTTTTTGA	XP_011512149.1:n.355+139_355+150delinsTTTTTTTTTTGA
XM_011513848.1:c.208+139_208+150delinsTTTTTTTTTTGA	XP_011512150.1:n.208+139_208+150delinsTTTTTTTTTTGA
XM_011513846.2:c.385+139_385+150delinsTTTTTTTTTTGA	XP_011512148.1:n.385+139_385+150delinsTTTTTTTTTTGA
XM_011513847.2:c.355+139_355+150delinsTTTTTTTTTTGA	XP_011512149.1:n.355+139_355+150delinsTTTTTTTTTTGA
XM_017008277.1:c.643+139_643+150delinsTTTTTTTTTTGA	XP_016863766.1:n.643+139_643+150delinsTTTTTTTTTTGA
XM_017008278.1:c.-36+139_-36+150delinsTTTTTTTTTTGA	XP_016863767.1:n.-36+139_-36+150delinsTTTTTTTTTTGA
NM_016955.4:c.388+139_388+150delinsTTTTTTTTTTGA MANE Select	NP_058651.3:n.388+139_388+150delinsTTTTTTTTTTGA