Canonical Allele Identifier: CA1445208237

Gene: SEPSECS

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156706_25156716delinsTCAAAAAAAAA , CM000666.2:g.25156706_25156716delinsTCAAAAAAAAA	GRCh38
NC_000004.11:g.25158328_25158338delinsTCAAAAAAAAA , CM000666.1:g.25158328_25158338delinsTCAAAAAAAAA	GRCh37
NC_000004.10:g.24767426_24767436delinsTCAAAAAAAAA	NCBI36
NG_028222.1:g.8867_8877delinsTTTTTTTTTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.388+140_388+150delinsTTTTTTTTTGA MANE Select	ENSP00000371535.2:n.388+140_388+150delinsTTTTTTTTTGA
ENST00000680581.1:c.388+140_388+150delinsTTTTTTTTTGA	ENSP00000506483.1:n.388+140_388+150delinsTTTTTTTTTGA
ENST00000680824.1:n.1604+140_1604+150delinsTTTTTTTTTGA
ENST00000681071.1:n.680+140_680+150delinsTTTTTTTTTGA
ENST00000681166.1:n.1435+140_1435+150delinsTTTTTTTTTGA
ENST00000681341.1:n.1529+140_1529+150delinsTTTTTTTTTGA
ENST00000681640.1:n.482+140_482+150delinsTTTTTTTTTGA
ENST00000681948.1:c.643+140_643+150delinsTTTTTTTTTGA	ENSP00000505991.1:n.643+140_643+150delinsTTTTTTTTTGA
ENST00000358971.7:c.*186+140_*186+150delinsTTTTTTTTTGA	ENSP00000351857.3:n.*186+140_*186+150delinsTTTTTTTTTGA
ENST00000382103.6:c.388+140_388+150delinsTTTTTTTTTGA	ENSP00000371535.2:n.388+140_388+150delinsTTTTTTTTTGA
ENST00000514585.5:c.*89+140_*89+150delinsTTTTTTTTTGA	ENSP00000421880.1:n.*89+140_*89+150delinsTTTTTTTTTGA
NM_016955.3:c.388+140_388+150delinsTTTTTTTTTGA	NP_058651.3:n.388+140_388+150delinsTTTTTTTTTGA
XM_005248168.2:c.151+140_151+150delinsTTTTTTTTTGA	XP_005248225.1:n.151+140_151+150delinsTTTTTTTTTGA
XM_006713965.2:c.208+140_208+150delinsTTTTTTTTTGA	XP_006714028.1:n.208+140_208+150delinsTTTTTTTTTGA
XM_011513846.1:c.385+140_385+150delinsTTTTTTTTTGA	XP_011512148.1:n.385+140_385+150delinsTTTTTTTTTGA
XM_011513847.1:c.355+140_355+150delinsTTTTTTTTTGA	XP_011512149.1:n.355+140_355+150delinsTTTTTTTTTGA
XM_011513848.1:c.208+140_208+150delinsTTTTTTTTTGA	XP_011512150.1:n.208+140_208+150delinsTTTTTTTTTGA
XM_011513846.2:c.385+140_385+150delinsTTTTTTTTTGA	XP_011512148.1:n.385+140_385+150delinsTTTTTTTTTGA
XM_011513847.2:c.355+140_355+150delinsTTTTTTTTTGA	XP_011512149.1:n.355+140_355+150delinsTTTTTTTTTGA
XM_017008277.1:c.643+140_643+150delinsTTTTTTTTTGA	XP_016863766.1:n.643+140_643+150delinsTTTTTTTTTGA
XM_017008278.1:c.-36+140_-36+150delinsTTTTTTTTTGA	XP_016863767.1:n.-36+140_-36+150delinsTTTTTTTTTGA
NM_016955.4:c.388+140_388+150delinsTTTTTTTTTGA MANE Select	NP_058651.3:n.388+140_388+150delinsTTTTTTTTTGA