Canonical Allele Identifier: CA793294416

Gene: SEPSECS

Linked Data

• dbSNP Id: rs1322180643
• gnomAD v3: 4-25156402-TTA-T
• gnomAD v4: 4-25156402-TTA-T
• MyVariant Identifiers: chr4:g.25158025_25158026del (hg19) ; chr4:g.25156403_25156404del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156403_25156404del , CM000666.2:g.25156403_25156404del	GRCh38
NC_000004.11:g.25158025_25158026del , CM000666.1:g.25158025_25158026del	GRCh37
NC_000004.10:g.24767123_24767124del	NCBI36
NG_028222.1:g.9179_9180del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.389-209_389-208del MANE Select	ENSP00000371535.2:n.389-209_389-208del
ENST00000680581.1:c.389-209_389-208del	ENSP00000506483.1:n.389-209_389-208del
ENST00000680824.1:n.1605-209_1605-208del
ENST00000681071.1:n.681-209_681-208del
ENST00000681166.1:n.1436-209_1436-208del
ENST00000681341.1:n.1530-209_1530-208del
ENST00000681640.1:n.483-209_483-208del
ENST00000681948.1:c.644-209_644-208del	ENSP00000505991.1:n.644-209_644-208del
ENST00000358971.7:c.*187-209_*187-208del	ENSP00000351857.3:n.*187-209_*187-208del
ENST00000382103.6:c.389-209_389-208del	ENSP00000371535.2:n.389-209_389-208del
ENST00000514585.5:c.*90-209_*90-208del	ENSP00000421880.1:n.*90-209_*90-208del
NM_016955.3:c.389-209_389-208del	NP_058651.3:n.389-209_389-208del
XM_005248168.2:c.152-209_152-208del	XP_005248225.1:n.152-209_152-208del
XM_006713965.2:c.209-209_209-208del	XP_006714028.1:n.209-209_209-208del
XM_011513846.1:c.386-209_386-208del	XP_011512148.1:n.386-209_386-208del
XM_011513847.1:c.356-209_356-208del	XP_011512149.1:n.356-209_356-208del
XM_011513848.1:c.209-209_209-208del	XP_011512150.1:n.209-209_209-208del
XM_011513846.2:c.386-209_386-208del	XP_011512148.1:n.386-209_386-208del
XM_011513847.2:c.356-209_356-208del	XP_011512149.1:n.356-209_356-208del
XM_017008277.1:c.644-209_644-208del	XP_016863766.1:n.644-209_644-208del
XM_017008278.1:c.-35-209_-35-208del	XP_016863767.1:n.-35-209_-35-208del
NM_016955.4:c.389-209_389-208del MANE Select	NP_058651.3:n.389-209_389-208del