Canonical Allele Identifier: CA2569311745

Gene: SEPSECS

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156411_25156414del , CM000666.2:g.25156411_25156414del	GRCh38
NC_000004.11:g.25158033_25158036del , CM000666.1:g.25158033_25158036del	GRCh37
NC_000004.10:g.24767131_24767134del	NCBI36
NG_028222.1:g.9176_9179del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.389-212_389-209del MANE Select	ENSP00000371535.2:n.389-212_389-209del
ENST00000680581.1:c.389-212_389-209del	ENSP00000506483.1:n.389-212_389-209del
ENST00000680824.1:n.1605-212_1605-209del
ENST00000681071.1:n.681-212_681-209del
ENST00000681166.1:n.1436-212_1436-209del
ENST00000681341.1:n.1530-212_1530-209del
ENST00000681640.1:n.483-212_483-209del
ENST00000681948.1:c.644-212_644-209del	ENSP00000505991.1:n.644-212_644-209del
ENST00000358971.7:c.*187-212_*187-209del	ENSP00000351857.3:n.*187-212_*187-209del
ENST00000382103.6:c.389-212_389-209del	ENSP00000371535.2:n.389-212_389-209del
ENST00000514585.5:c.*90-212_*90-209del	ENSP00000421880.1:n.*90-212_*90-209del
NM_016955.3:c.389-212_389-209del	NP_058651.3:n.389-212_389-209del
XM_005248168.2:c.152-212_152-209del	XP_005248225.1:n.152-212_152-209del
XM_006713965.2:c.209-212_209-209del	XP_006714028.1:n.209-212_209-209del
XM_011513846.1:c.386-212_386-209del	XP_011512148.1:n.386-212_386-209del
XM_011513847.1:c.356-212_356-209del	XP_011512149.1:n.356-212_356-209del
XM_011513848.1:c.209-212_209-209del	XP_011512150.1:n.209-212_209-209del
XM_011513846.2:c.386-212_386-209del	XP_011512148.1:n.386-212_386-209del
XM_011513847.2:c.356-212_356-209del	XP_011512149.1:n.356-212_356-209del
XM_017008277.1:c.644-212_644-209del	XP_016863766.1:n.644-212_644-209del
XM_017008278.1:c.-35-212_-35-209del	XP_016863767.1:n.-35-212_-35-209del
NM_016955.4:c.389-212_389-209del MANE Select	NP_058651.3:n.389-212_389-209del