Canonical Allele Identifier: CA3052065394

Gene: SEPSECS

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156856_25156857insCTT , CM000666.2:g.25156856_25156857insCTT	GRCh38
NC_000004.11:g.25158478_25158479insCTT , CM000666.1:g.25158478_25158479insCTT	GRCh37
NC_000004.10:g.24767576_24767577insCTT	NCBI36
NG_028222.1:g.8726_8727insAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.387_388insAAG MANE Select	ENSP00000371535.2:p.Ala129_Gly130insLys
ENST00000680581.1:c.387_388insAAG	ENSP00000506483.1:p.Ala129_Gly130insLys
ENST00000680824.1:n.1603_1604insAAG
ENST00000681071.1:n.679_680insAAG
ENST00000681166.1:n.1434_1435insAAG
ENST00000681341.1:n.1528_1529insAAG
ENST00000681640.1:n.481_482insAAG
ENST00000681948.1:c.642_643insAAG	ENSP00000505991.1:p.Ala214_Gly215insLys
ENST00000358971.7:c.*185_*186insAAG	ENSP00000351857.3:n.*185_*186insAAG
ENST00000382103.6:c.387_388insAAG	ENSP00000371535.2:p.Ala129_Gly130insLys
ENST00000514585.5:c.*88_*89insAAG	ENSP00000421880.1:n.*88_*89insAAG
NM_016955.3:c.387_388insAAG	NP_058651.3:p.Ala129_Gly130insLys
XM_005248168.2:c.150_151insAAG	XP_005248225.1:p.Ala50_Gly51insLys
XM_006713965.2:c.207_208insAAG	XP_006714028.1:p.Ala69_Gly70insLys
XM_011513846.1:c.384_385insAAG	XP_011512148.1:p.Ala128_Gly129insLys
XM_011513847.1:c.354_355insAAG	XP_011512149.1:p.Ala118_Gly119insLys
XM_011513848.1:c.207_208insAAG	XP_011512150.1:p.Ala69_Gly70insLys
XM_011513846.2:c.384_385insAAG	XP_011512148.1:p.Ala128_Gly129insLys
XM_011513847.2:c.354_355insAAG	XP_011512149.1:p.Ala118_Gly119insLys
XM_017008277.1:c.642_643insAAG	XP_016863766.1:p.Ala214_Gly215insLys
XM_017008278.1:c.-37_-36insAAG	XP_016863767.1:n.-37_-36insAAG
NM_016955.4:c.387_388insAAG MANE Select	NP_058651.3:p.Ala129_Gly130insLys