Canonical Allele Identifier: CA1060328064

Gene: SEPSECS

Linked Data

• gnomAD v3: 4-25156740-T-TAAAAA
• gnomAD v4: 4-25156740-T-TAAAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156740_25156741insAAAAA , CM000666.2:g.25156740_25156741insAAAAA	GRCh38
NC_000004.11:g.25158362_25158363insAAAAA , CM000666.1:g.25158362_25158363insAAAAA	GRCh37
NC_000004.10:g.24767460_24767461insAAAAA	NCBI36
NG_028222.1:g.8842_8843insTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.388+115_388+116insTTTTT MANE Select	ENSP00000371535.2:n.388+115_388+116insTTTTT
ENST00000680581.1:c.388+115_388+116insTTTTT	ENSP00000506483.1:n.388+115_388+116insTTTTT
ENST00000680824.1:n.1604+115_1604+116insTTTTT
ENST00000681071.1:n.680+115_680+116insTTTTT
ENST00000681166.1:n.1435+115_1435+116insTTTTT
ENST00000681341.1:n.1529+115_1529+116insTTTTT
ENST00000681640.1:n.482+115_482+116insTTTTT
ENST00000681948.1:c.643+115_643+116insTTTTT	ENSP00000505991.1:n.643+115_643+116insTTTTT
ENST00000358971.7:c.*186+115_*186+116insTTTTT	ENSP00000351857.3:n.*186+115_*186+116insTTTTT
ENST00000382103.6:c.388+115_388+116insTTTTT	ENSP00000371535.2:n.388+115_388+116insTTTTT
ENST00000514585.5:c.*89+115_*89+116insTTTTT	ENSP00000421880.1:n.*89+115_*89+116insTTTTT
NM_016955.3:c.388+115_388+116insTTTTT	NP_058651.3:n.388+115_388+116insTTTTT
XM_005248168.2:c.151+115_151+116insTTTTT	XP_005248225.1:n.151+115_151+116insTTTTT
XM_006713965.2:c.208+115_208+116insTTTTT	XP_006714028.1:n.208+115_208+116insTTTTT
XM_011513846.1:c.385+115_385+116insTTTTT	XP_011512148.1:n.385+115_385+116insTTTTT
XM_011513847.1:c.355+115_355+116insTTTTT	XP_011512149.1:n.355+115_355+116insTTTTT
XM_011513848.1:c.208+115_208+116insTTTTT	XP_011512150.1:n.208+115_208+116insTTTTT
XM_011513846.2:c.385+115_385+116insTTTTT	XP_011512148.1:n.385+115_385+116insTTTTT
XM_011513847.2:c.355+115_355+116insTTTTT	XP_011512149.1:n.355+115_355+116insTTTTT
XM_017008277.1:c.643+115_643+116insTTTTT	XP_016863766.1:n.643+115_643+116insTTTTT
XM_017008278.1:c.-36+115_-36+116insTTTTT	XP_016863767.1:n.-36+115_-36+116insTTTTT
NM_016955.4:c.388+115_388+116insTTTTT MANE Select	NP_058651.3:n.388+115_388+116insTTTTT