Canonical Allele Identifier: CA1445204200

Gene: SEPSECS

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25120543_25120546delinsGGTT , CM000666.2:g.25120543_25120546delinsGGTT	GRCh38
NC_000004.11:g.25122165_25122168delinsGGTT , CM000666.1:g.25122165_25122168delinsGGTT	GRCh37
NC_000004.10:g.24731263_24731266delinsGGTT	NCBI36
NG_028222.1:g.45037_45040delinsAACC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.*3385_*3388delinsAACC MANE Select	ENSP00000371535.2:n.*3385_*3388delinsAACC
ENST00000680581.1:c.*3765_*3768delinsAACC	ENSP00000506483.1:n.*3765_*3768delinsAACC
ENST00000680824.1:n.6107_6110delinsAACC
ENST00000681071.1:n.5183_5186delinsAACC
ENST00000681341.1:n.5938_5941delinsAACC
ENST00000681374.1:n.4247_4250delinsAACC
ENST00000681948.1:c.*3385_*3388delinsAACC	ENSP00000505991.1:n.*3385_*3388delinsAACC
ENST00000382103.6:c.*3385_*3388delinsAACC	ENSP00000371535.2:n.*3385_*3388delinsAACC
NM_016955.3:c.*3385_*3388delinsAACC	NP_058651.3:n.*3385_*3388delinsAACC
XM_005248168.2:c.*3385_*3388delinsAACC	XP_005248225.1:n.*3385_*3388delinsAACC
XM_006713965.2:c.*3385_*3388delinsAACC	XP_006714028.1:n.*3385_*3388delinsAACC
XM_011513846.1:c.*3385_*3388delinsAACC	XP_011512148.1:n.*3385_*3388delinsAACC
XM_011513847.1:c.*3385_*3388delinsAACC	XP_011512149.1:n.*3385_*3388delinsAACC
XM_011513848.1:c.*3385_*3388delinsAACC	XP_011512150.1:n.*3385_*3388delinsAACC
XM_011513846.2:c.*3385_*3388delinsAACC	XP_011512148.1:n.*3385_*3388delinsAACC
XM_011513847.2:c.*3385_*3388delinsAACC	XP_011512149.1:n.*3385_*3388delinsAACC
XM_017008277.1:c.*3385_*3388delinsAACC	XP_016863766.1:n.*3385_*3388delinsAACC
XM_017008278.1:c.*3385_*3388delinsAACC	XP_016863767.1:n.*3385_*3388delinsAACC
NM_016955.4:c.*3385_*3388delinsAACC MANE Select	NP_058651.3:n.*3385_*3388delinsAACC