Canonical Allele Identifier: CA1445208224

Gene: SEPSECS

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156706_25156715delinsTCAAAAAAAA , CM000666.2:g.25156706_25156715delinsTCAAAAAAAA	GRCh38
NC_000004.11:g.25158328_25158337delinsTCAAAAAAAA , CM000666.1:g.25158328_25158337delinsTCAAAAAAAA	GRCh37
NC_000004.10:g.24767426_24767435delinsTCAAAAAAAA	NCBI36
NG_028222.1:g.8868_8877delinsTTTTTTTTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.388+141_388+150delinsTTTTTTTTGA MANE Select	ENSP00000371535.2:n.388+141_388+150delinsTTTTTTTTGA
ENST00000680581.1:c.388+141_388+150delinsTTTTTTTTGA	ENSP00000506483.1:n.388+141_388+150delinsTTTTTTTTGA
ENST00000680824.1:n.1604+141_1604+150delinsTTTTTTTTGA
ENST00000681071.1:n.680+141_680+150delinsTTTTTTTTGA
ENST00000681166.1:n.1435+141_1435+150delinsTTTTTTTTGA
ENST00000681341.1:n.1529+141_1529+150delinsTTTTTTTTGA
ENST00000681640.1:n.482+141_482+150delinsTTTTTTTTGA
ENST00000681948.1:c.643+141_643+150delinsTTTTTTTTGA	ENSP00000505991.1:n.643+141_643+150delinsTTTTTTTTGA
ENST00000358971.7:c.*186+141_*186+150delinsTTTTTTTTGA	ENSP00000351857.3:n.*186+141_*186+150delinsTTTTTTTTGA
ENST00000382103.6:c.388+141_388+150delinsTTTTTTTTGA	ENSP00000371535.2:n.388+141_388+150delinsTTTTTTTTGA
ENST00000514585.5:c.*89+141_*89+150delinsTTTTTTTTGA	ENSP00000421880.1:n.*89+141_*89+150delinsTTTTTTTTGA
NM_016955.3:c.388+141_388+150delinsTTTTTTTTGA	NP_058651.3:n.388+141_388+150delinsTTTTTTTTGA
XM_005248168.2:c.151+141_151+150delinsTTTTTTTTGA	XP_005248225.1:n.151+141_151+150delinsTTTTTTTTGA
XM_006713965.2:c.208+141_208+150delinsTTTTTTTTGA	XP_006714028.1:n.208+141_208+150delinsTTTTTTTTGA
XM_011513846.1:c.385+141_385+150delinsTTTTTTTTGA	XP_011512148.1:n.385+141_385+150delinsTTTTTTTTGA
XM_011513847.1:c.355+141_355+150delinsTTTTTTTTGA	XP_011512149.1:n.355+141_355+150delinsTTTTTTTTGA
XM_011513848.1:c.208+141_208+150delinsTTTTTTTTGA	XP_011512150.1:n.208+141_208+150delinsTTTTTTTTGA
XM_011513846.2:c.385+141_385+150delinsTTTTTTTTGA	XP_011512148.1:n.385+141_385+150delinsTTTTTTTTGA
XM_011513847.2:c.355+141_355+150delinsTTTTTTTTGA	XP_011512149.1:n.355+141_355+150delinsTTTTTTTTGA
XM_017008277.1:c.643+141_643+150delinsTTTTTTTTGA	XP_016863766.1:n.643+141_643+150delinsTTTTTTTTGA
XM_017008278.1:c.-36+141_-36+150delinsTTTTTTTTGA	XP_016863767.1:n.-36+141_-36+150delinsTTTTTTTTGA
NM_016955.4:c.388+141_388+150delinsTTTTTTTTGA MANE Select	NP_058651.3:n.388+141_388+150delinsTTTTTTTTGA