Canonical Allele Identifier: CA2760775022

Gene: SEPSECS

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156706_25156714del , CM000666.2:g.25156706_25156714del	GRCh38
NC_000004.11:g.25158328_25158336del , CM000666.1:g.25158328_25158336del	GRCh37
NC_000004.10:g.24767426_24767434del	NCBI36
NG_028222.1:g.8869_8877del

Transcript Alleles

HGVS	Amino-acid change
ENST00000382103.7:c.388+142_388+150del MANE Select	ENSP00000371535.2:n.388+142_388+150del
ENST00000680581.1:c.388+142_388+150del	ENSP00000506483.1:n.388+142_388+150del
ENST00000680824.1:n.1604+142_1604+150del
ENST00000681071.1:n.680+142_680+150del
ENST00000681166.1:n.1435+142_1435+150del
ENST00000681341.1:n.1529+142_1529+150del
ENST00000681640.1:n.482+142_482+150del
ENST00000681948.1:c.643+142_643+150del	ENSP00000505991.1:n.643+142_643+150del
ENST00000358971.7:c.*186+142_*186+150del	ENSP00000351857.3:n.*186+142_*186+150del
ENST00000382103.6:c.388+142_388+150del	ENSP00000371535.2:n.388+142_388+150del
ENST00000514585.5:c.*89+142_*89+150del	ENSP00000421880.1:n.*89+142_*89+150del
NM_016955.3:c.388+142_388+150del	NP_058651.3:n.388+142_388+150del
XM_005248168.2:c.151+142_151+150del	XP_005248225.1:n.151+142_151+150del
XM_006713965.2:c.208+142_208+150del	XP_006714028.1:n.208+142_208+150del
XM_011513846.1:c.385+142_385+150del	XP_011512148.1:n.385+142_385+150del
XM_011513847.1:c.355+142_355+150del	XP_011512149.1:n.355+142_355+150del
XM_011513848.1:c.208+142_208+150del	XP_011512150.1:n.208+142_208+150del
XM_011513846.2:c.385+142_385+150del	XP_011512148.1:n.385+142_385+150del
XM_011513847.2:c.355+142_355+150del	XP_011512149.1:n.355+142_355+150del
XM_017008277.1:c.643+142_643+150del	XP_016863766.1:n.643+142_643+150del
XM_017008278.1:c.-36+142_-36+150del	XP_016863767.1:n.-36+142_-36+150del
NM_016955.4:c.388+142_388+150del MANE Select	NP_058651.3:n.388+142_388+150del