Canonical Allele Identifier: CA2760774940

Gene: SEPSECS

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156347_25156348del , CM000666.2:g.25156347_25156348del	GRCh38
NC_000004.11:g.25157969_25157970del , CM000666.1:g.25157969_25157970del	GRCh37
NC_000004.10:g.24767067_24767068del	NCBI36
NG_028222.1:g.9235_9236del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.389-153_389-152del MANE Select	ENSP00000371535.2:n.389-153_389-152del
ENST00000680581.1:c.389-153_389-152del	ENSP00000506483.1:n.389-153_389-152del
ENST00000680824.1:n.1605-153_1605-152del
ENST00000681071.1:n.681-153_681-152del
ENST00000681166.1:n.1436-153_1436-152del
ENST00000681341.1:n.1530-153_1530-152del
ENST00000681640.1:n.483-153_483-152del
ENST00000681948.1:c.644-153_644-152del	ENSP00000505991.1:n.644-153_644-152del
ENST00000358971.7:c.*187-153_*187-152del	ENSP00000351857.3:n.*187-153_*187-152del
ENST00000382103.6:c.389-153_389-152del	ENSP00000371535.2:n.389-153_389-152del
ENST00000514585.5:c.*90-153_*90-152del	ENSP00000421880.1:n.*90-153_*90-152del
NM_016955.3:c.389-153_389-152del	NP_058651.3:n.389-153_389-152del
XM_005248168.2:c.152-153_152-152del	XP_005248225.1:n.152-153_152-152del
XM_006713965.2:c.209-153_209-152del	XP_006714028.1:n.209-153_209-152del
XM_011513846.1:c.386-153_386-152del	XP_011512148.1:n.386-153_386-152del
XM_011513847.1:c.356-153_356-152del	XP_011512149.1:n.356-153_356-152del
XM_011513848.1:c.209-153_209-152del	XP_011512150.1:n.209-153_209-152del
XM_011513846.2:c.386-153_386-152del	XP_011512148.1:n.386-153_386-152del
XM_011513847.2:c.356-153_356-152del	XP_011512149.1:n.356-153_356-152del
XM_017008277.1:c.644-153_644-152del	XP_016863766.1:n.644-153_644-152del
XM_017008278.1:c.-35-153_-35-152del	XP_016863767.1:n.-35-153_-35-152del
NM_016955.4:c.389-153_389-152del MANE Select	NP_058651.3:n.389-153_389-152del