Canonical Allele Identifier: CA2670197175

Gene: SEPSECS

Linked Data

• gnomAD v4: 4-25156736-G-GTCTTTTCAA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156736_25156737insTCTTTTCAA , CM000666.2:g.25156736_25156737insTCTTTTCAA	GRCh38
NC_000004.11:g.25158358_25158359insTCTTTTCAA , CM000666.1:g.25158358_25158359insTCTTTTCAA	GRCh37
NC_000004.10:g.24767456_24767457insTCTTTTCAA	NCBI36
NG_028222.1:g.8846_8847insTTGAAAAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.388+119_388+120insTTGAAAAGA MANE Select	ENSP00000371535.2:n.388+119_388+120insTTGAAAAGA
ENST00000680581.1:c.388+119_388+120insTTGAAAAGA	ENSP00000506483.1:n.388+119_388+120insTTGAAAAGA
ENST00000680824.1:n.1604+119_1604+120insTTGAAAAGA
ENST00000681071.1:n.680+119_680+120insTTGAAAAGA
ENST00000681166.1:n.1435+119_1435+120insTTGAAAAGA
ENST00000681341.1:n.1529+119_1529+120insTTGAAAAGA
ENST00000681640.1:n.482+119_482+120insTTGAAAAGA
ENST00000681948.1:c.643+119_643+120insTTGAAAAGA	ENSP00000505991.1:n.643+119_643+120insTTGAAAAGA
ENST00000358971.7:c.*186+119_*186+120insTTGAAAAGA	ENSP00000351857.3:n.*186+119_*186+120insTTGAAAAGA
ENST00000382103.6:c.388+119_388+120insTTGAAAAGA	ENSP00000371535.2:n.388+119_388+120insTTGAAAAGA
ENST00000514585.5:c.*89+119_*89+120insTTGAAAAGA	ENSP00000421880.1:n.*89+119_*89+120insTTGAAAAGA
NM_016955.3:c.388+119_388+120insTTGAAAAGA	NP_058651.3:n.388+119_388+120insTTGAAAAGA
XM_005248168.2:c.151+119_151+120insTTGAAAAGA	XP_005248225.1:n.151+119_151+120insTTGAAAAGA
XM_006713965.2:c.208+119_208+120insTTGAAAAGA	XP_006714028.1:n.208+119_208+120insTTGAAAAGA
XM_011513846.1:c.385+119_385+120insTTGAAAAGA	XP_011512148.1:n.385+119_385+120insTTGAAAAGA
XM_011513847.1:c.355+119_355+120insTTGAAAAGA	XP_011512149.1:n.355+119_355+120insTTGAAAAGA
XM_011513848.1:c.208+119_208+120insTTGAAAAGA	XP_011512150.1:n.208+119_208+120insTTGAAAAGA
XM_011513846.2:c.385+119_385+120insTTGAAAAGA	XP_011512148.1:n.385+119_385+120insTTGAAAAGA
XM_011513847.2:c.355+119_355+120insTTGAAAAGA	XP_011512149.1:n.355+119_355+120insTTGAAAAGA
XM_017008277.1:c.643+119_643+120insTTGAAAAGA	XP_016863766.1:n.643+119_643+120insTTGAAAAGA
XM_017008278.1:c.-36+119_-36+120insTTGAAAAGA	XP_016863767.1:n.-36+119_-36+120insTTGAAAAGA
NM_016955.4:c.388+119_388+120insTTGAAAAGA MANE Select	NP_058651.3:n.388+119_388+120insTTGAAAAGA