Canonical Allele Identifier: CA550289860

Gene: SEPSECS

Linked Data

• gnomAD v2: 4-25158368-C-CAA
• gnomAD v3: 4-25156746-C-CAA
• gnomAD v4: 4-25156746-C-CAA
• MyVariant Identifiers: chr4:g.25158368_25158369insAA (hg19) ; chr4:g.25156746_25156747insAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156749_25156750dup , CM000666.2:g.25156749_25156750dup	GRCh38
NC_000004.11:g.25158371_25158372dup , CM000666.1:g.25158371_25158372dup	GRCh37
NC_000004.10:g.24767469_24767470dup	NCBI36
NG_028222.1:g.8835_8836dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.388+108_388+109dup MANE Select	ENSP00000371535.2:n.388+108_388+109dup
ENST00000680581.1:c.388+108_388+109dup	ENSP00000506483.1:n.388+108_388+109dup
ENST00000680824.1:n.1604+108_1604+109dup
ENST00000681071.1:n.680+108_680+109dup
ENST00000681166.1:n.1435+108_1435+109dup
ENST00000681341.1:n.1529+108_1529+109dup
ENST00000681640.1:n.482+108_482+109dup
ENST00000681948.1:c.643+108_643+109dup	ENSP00000505991.1:n.643+108_643+109dup
ENST00000358971.7:c.*186+108_*186+109dup	ENSP00000351857.3:n.*186+108_*186+109dup
ENST00000382103.6:c.388+108_388+109dup	ENSP00000371535.2:n.388+108_388+109dup
ENST00000514585.5:c.*89+108_*89+109dup	ENSP00000421880.1:n.*89+108_*89+109dup
NM_016955.3:c.388+108_388+109dup	NP_058651.3:n.388+108_388+109dup
XM_005248168.2:c.151+108_151+109dup	XP_005248225.1:n.151+108_151+109dup
XM_006713965.2:c.208+108_208+109dup	XP_006714028.1:n.208+108_208+109dup
XM_011513846.1:c.385+108_385+109dup	XP_011512148.1:n.385+108_385+109dup
XM_011513847.1:c.355+108_355+109dup	XP_011512149.1:n.355+108_355+109dup
XM_011513848.1:c.208+108_208+109dup	XP_011512150.1:n.208+108_208+109dup
XM_011513846.2:c.385+108_385+109dup	XP_011512148.1:n.385+108_385+109dup
XM_011513847.2:c.355+108_355+109dup	XP_011512149.1:n.355+108_355+109dup
XM_017008277.1:c.643+108_643+109dup	XP_016863766.1:n.643+108_643+109dup
XM_017008278.1:c.-36+108_-36+109dup	XP_016863767.1:n.-36+108_-36+109dup
NM_016955.4:c.388+108_388+109dup MANE Select	NP_058651.3:n.388+108_388+109dup