Canonical Allele Identifier: CA2705252577

Gene: SEPSECS

Linked Data

• dbSNP Id: rs2109035192

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156706_25156707del , CM000666.2:g.25156706_25156707del	GRCh38
NC_000004.11:g.25158328_25158329del , CM000666.1:g.25158328_25158329del	GRCh37
NC_000004.10:g.24767426_24767427del	NCBI36
NG_028222.1:g.8878_8879del

Transcript Alleles

HGVS	Amino-acid change
ENST00000382103.7:c.388+151_388+152del MANE Select	ENSP00000371535.2:n.388+151_388+152del
ENST00000680581.1:c.388+151_388+152del	ENSP00000506483.1:n.388+151_388+152del
ENST00000680824.1:n.1604+151_1604+152del
ENST00000681071.1:n.680+151_680+152del
ENST00000681166.1:n.1435+151_1435+152del
ENST00000681341.1:n.1529+151_1529+152del
ENST00000681640.1:n.482+151_482+152del
ENST00000681948.1:c.643+151_643+152del	ENSP00000505991.1:n.643+151_643+152del
ENST00000358971.7:c.*186+151_*186+152del	ENSP00000351857.3:n.*186+151_*186+152del
ENST00000382103.6:c.388+151_388+152del	ENSP00000371535.2:n.388+151_388+152del
ENST00000514585.5:c.*89+151_*89+152del	ENSP00000421880.1:n.*89+151_*89+152del
NM_016955.3:c.388+151_388+152del	NP_058651.3:n.388+151_388+152del
XM_005248168.2:c.151+151_151+152del	XP_005248225.1:n.151+151_151+152del
XM_006713965.2:c.208+151_208+152del	XP_006714028.1:n.208+151_208+152del
XM_011513846.1:c.385+151_385+152del	XP_011512148.1:n.385+151_385+152del
XM_011513847.1:c.355+151_355+152del	XP_011512149.1:n.355+151_355+152del
XM_011513848.1:c.208+151_208+152del	XP_011512150.1:n.208+151_208+152del
XM_011513846.2:c.385+151_385+152del	XP_011512148.1:n.385+151_385+152del
XM_011513847.2:c.355+151_355+152del	XP_011512149.1:n.355+151_355+152del
XM_017008277.1:c.643+151_643+152del	XP_016863766.1:n.643+151_643+152del
XM_017008278.1:c.-36+151_-36+152del	XP_016863767.1:n.-36+151_-36+152del
NM_016955.4:c.388+151_388+152del MANE Select	NP_058651.3:n.388+151_388+152del