Canonical Allele Identifier: CA550289866

Gene: SEPSECS

Linked Data

• dbSNP Id: rs1560336745
• gnomAD v2: 4-25158463-T-TAAG
• gnomAD v4: 4-25156841-T-TAAG
• MyVariant Identifiers: chr4:g.25158463_25158464insAAG (hg19) ; chr4:g.25156841_25156842insAAG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156843_25156845dup , CM000666.2:g.25156843_25156845dup	GRCh38
NC_000004.11:g.25158465_25158467dup , CM000666.1:g.25158465_25158467dup	GRCh37
NC_000004.10:g.24767563_24767565dup	NCBI36
NG_028222.1:g.8739_8741dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.388+12_388+14dup MANE Select	ENSP00000371535.2:n.388+12_388+14dup
ENST00000680581.1:c.388+12_388+14dup	ENSP00000506483.1:n.388+12_388+14dup
ENST00000680824.1:n.1604+12_1604+14dup
ENST00000681071.1:n.680+12_680+14dup
ENST00000681166.1:n.1435+12_1435+14dup
ENST00000681341.1:n.1529+12_1529+14dup
ENST00000681640.1:n.482+12_482+14dup
ENST00000681948.1:c.643+12_643+14dup	ENSP00000505991.1:n.643+12_643+14dup
ENST00000358971.7:c.*186+12_*186+14dup	ENSP00000351857.3:n.*186+12_*186+14dup
ENST00000382103.6:c.388+12_388+14dup	ENSP00000371535.2:n.388+12_388+14dup
ENST00000514585.5:c.*89+12_*89+14dup	ENSP00000421880.1:n.*89+12_*89+14dup
NM_016955.3:c.388+12_388+14dup	NP_058651.3:n.388+12_388+14dup
XM_005248168.2:c.151+12_151+14dup	XP_005248225.1:n.151+12_151+14dup
XM_006713965.2:c.208+12_208+14dup	XP_006714028.1:n.208+12_208+14dup
XM_011513846.1:c.385+12_385+14dup	XP_011512148.1:n.385+12_385+14dup
XM_011513847.1:c.355+12_355+14dup	XP_011512149.1:n.355+12_355+14dup
XM_011513848.1:c.208+12_208+14dup	XP_011512150.1:n.208+12_208+14dup
XM_011513846.2:c.385+12_385+14dup	XP_011512148.1:n.385+12_385+14dup
XM_011513847.2:c.355+12_355+14dup	XP_011512149.1:n.355+12_355+14dup
XM_017008277.1:c.643+12_643+14dup	XP_016863766.1:n.643+12_643+14dup
XM_017008278.1:c.-36+12_-36+14dup	XP_016863767.1:n.-36+12_-36+14dup
NM_016955.4:c.388+12_388+14dup MANE Select	NP_058651.3:n.388+12_388+14dup