Canonical Allele Identifier: CA1060328078

Gene: SEPSECS

Linked Data

• gnomAD v3: 4-25156746-C-CAAAAAAA
• gnomAD v4: 4-25156746-C-CAAAAAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156750_25156751insAAAAAAA , CM000666.2:g.25156750_25156751insAAAAAAA	GRCh38
NC_000004.11:g.25158372_25158373insAAAAAAA , CM000666.1:g.25158372_25158373insAAAAAAA	GRCh37
NC_000004.10:g.24767470_24767471insAAAAAAA	NCBI36
NG_028222.1:g.8836_8837insTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.388+109_388+110insTTTTTTT MANE Select	ENSP00000371535.2:n.388+109_388+110insTTTTTTT
ENST00000680581.1:c.388+109_388+110insTTTTTTT	ENSP00000506483.1:n.388+109_388+110insTTTTTTT
ENST00000680824.1:n.1604+109_1604+110insTTTTTTT
ENST00000681071.1:n.680+109_680+110insTTTTTTT
ENST00000681166.1:n.1435+109_1435+110insTTTTTTT
ENST00000681341.1:n.1529+109_1529+110insTTTTTTT
ENST00000681640.1:n.482+109_482+110insTTTTTTT
ENST00000681948.1:c.643+109_643+110insTTTTTTT	ENSP00000505991.1:n.643+109_643+110insTTTTTTT
ENST00000358971.7:c.*186+109_*186+110insTTTTTTT	ENSP00000351857.3:n.*186+109_*186+110insTTTTTTT
ENST00000382103.6:c.388+109_388+110insTTTTTTT	ENSP00000371535.2:n.388+109_388+110insTTTTTTT
ENST00000514585.5:c.*89+109_*89+110insTTTTTTT	ENSP00000421880.1:n.*89+109_*89+110insTTTTTTT
NM_016955.3:c.388+109_388+110insTTTTTTT	NP_058651.3:n.388+109_388+110insTTTTTTT
XM_005248168.2:c.151+109_151+110insTTTTTTT	XP_005248225.1:n.151+109_151+110insTTTTTTT
XM_006713965.2:c.208+109_208+110insTTTTTTT	XP_006714028.1:n.208+109_208+110insTTTTTTT
XM_011513846.1:c.385+109_385+110insTTTTTTT	XP_011512148.1:n.385+109_385+110insTTTTTTT
XM_011513847.1:c.355+109_355+110insTTTTTTT	XP_011512149.1:n.355+109_355+110insTTTTTTT
XM_011513848.1:c.208+109_208+110insTTTTTTT	XP_011512150.1:n.208+109_208+110insTTTTTTT
XM_011513846.2:c.385+109_385+110insTTTTTTT	XP_011512148.1:n.385+109_385+110insTTTTTTT
XM_011513847.2:c.355+109_355+110insTTTTTTT	XP_011512149.1:n.355+109_355+110insTTTTTTT
XM_017008277.1:c.643+109_643+110insTTTTTTT	XP_016863766.1:n.643+109_643+110insTTTTTTT
XM_017008278.1:c.-36+109_-36+110insTTTTTTT	XP_016863767.1:n.-36+109_-36+110insTTTTTTT
NM_016955.4:c.388+109_388+110insTTTTTTT MANE Select	NP_058651.3:n.388+109_388+110insTTTTTTT