Canonical Allele Identifier: CA1445207917

Gene: SEPSECS

Linked Data

• dbSNP Id: rs1311033645

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156556_25156558del , CM000666.2:g.25156556_25156558del	GRCh38
NC_000004.11:g.25158178_25158180del , CM000666.1:g.25158178_25158180del	GRCh37
NC_000004.10:g.24767276_24767278del	NCBI36
NG_028222.1:g.9031_9033del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.388+304_388+306del MANE Select	ENSP00000371535.2:n.388+304_388+306del
ENST00000680581.1:c.388+304_388+306del	ENSP00000506483.1:n.388+304_388+306del
ENST00000680824.1:n.1604+304_1604+306del
ENST00000681071.1:n.680+304_680+306del
ENST00000681166.1:n.1435+304_1435+306del
ENST00000681341.1:n.1529+304_1529+306del
ENST00000681640.1:n.482+304_482+306del
ENST00000681948.1:c.643+304_643+306del	ENSP00000505991.1:n.643+304_643+306del
ENST00000358971.7:c.*186+304_*186+306del	ENSP00000351857.3:n.*186+304_*186+306del
ENST00000382103.6:c.388+304_388+306del	ENSP00000371535.2:n.388+304_388+306del
ENST00000514585.5:c.*89+304_*89+306del	ENSP00000421880.1:n.*89+304_*89+306del
NM_016955.3:c.388+304_388+306del	NP_058651.3:n.388+304_388+306del
XM_005248168.2:c.151+304_151+306del	XP_005248225.1:n.151+304_151+306del
XM_006713965.2:c.208+304_208+306del	XP_006714028.1:n.208+304_208+306del
XM_011513846.1:c.385+304_385+306del	XP_011512148.1:n.385+304_385+306del
XM_011513847.1:c.355+304_355+306del	XP_011512149.1:n.355+304_355+306del
XM_011513848.1:c.208+304_208+306del	XP_011512150.1:n.208+304_208+306del
XM_011513846.2:c.385+304_385+306del	XP_011512148.1:n.385+304_385+306del
XM_011513847.2:c.355+304_355+306del	XP_011512149.1:n.355+304_355+306del
XM_017008277.1:c.643+304_643+306del	XP_016863766.1:n.643+304_643+306del
XM_017008278.1:c.-36+304_-36+306del	XP_016863767.1:n.-36+304_-36+306del
NM_016955.4:c.388+304_388+306del MANE Select	NP_058651.3:n.388+304_388+306del