Canonical Allele Identifier: CA2760775117

Gene: SEPSECS

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156736_25156740del , CM000666.2:g.25156736_25156740del	GRCh38
NC_000004.11:g.25158358_25158362del , CM000666.1:g.25158358_25158362del	GRCh37
NC_000004.10:g.24767456_24767460del	NCBI36
NG_028222.1:g.8843_8847del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.388+116_388+120del MANE Select	ENSP00000371535.2:n.388+116_388+120del
ENST00000680581.1:c.388+116_388+120del	ENSP00000506483.1:n.388+116_388+120del
ENST00000680824.1:n.1604+116_1604+120del
ENST00000681071.1:n.680+116_680+120del
ENST00000681166.1:n.1435+116_1435+120del
ENST00000681341.1:n.1529+116_1529+120del
ENST00000681640.1:n.482+116_482+120del
ENST00000681948.1:c.643+116_643+120del	ENSP00000505991.1:n.643+116_643+120del
ENST00000358971.7:c.*186+116_*186+120del	ENSP00000351857.3:n.*186+116_*186+120del
ENST00000382103.6:c.388+116_388+120del	ENSP00000371535.2:n.388+116_388+120del
ENST00000514585.5:c.*89+116_*89+120del	ENSP00000421880.1:n.*89+116_*89+120del
NM_016955.3:c.388+116_388+120del	NP_058651.3:n.388+116_388+120del
XM_005248168.2:c.151+116_151+120del	XP_005248225.1:n.151+116_151+120del
XM_006713965.2:c.208+116_208+120del	XP_006714028.1:n.208+116_208+120del
XM_011513846.1:c.385+116_385+120del	XP_011512148.1:n.385+116_385+120del
XM_011513847.1:c.355+116_355+120del	XP_011512149.1:n.355+116_355+120del
XM_011513848.1:c.208+116_208+120del	XP_011512150.1:n.208+116_208+120del
XM_011513846.2:c.385+116_385+120del	XP_011512148.1:n.385+116_385+120del
XM_011513847.2:c.355+116_355+120del	XP_011512149.1:n.355+116_355+120del
XM_017008277.1:c.643+116_643+120del	XP_016863766.1:n.643+116_643+120del
XM_017008278.1:c.-36+116_-36+120del	XP_016863767.1:n.-36+116_-36+120del
NM_016955.4:c.388+116_388+120del MANE Select	NP_058651.3:n.388+116_388+120del