Canonical Allele Identifier: CA917150676

Gene: SEPSECS

Linked Data

• dbSNP Id: rs1577631496

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156719_25156720insG , CM000666.2:g.25156719_25156720insG	GRCh38
NC_000004.11:g.25158341_25158342insG , CM000666.1:g.25158341_25158342insG	GRCh37
NC_000004.10:g.24767439_24767440insG	NCBI36
NG_028222.1:g.8863_8864insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.388+136_388+137insC MANE Select	ENSP00000371535.2:n.388+136_388+137insC
ENST00000680581.1:c.388+136_388+137insC	ENSP00000506483.1:n.388+136_388+137insC
ENST00000680824.1:n.1604+136_1604+137insC
ENST00000681071.1:n.680+136_680+137insC
ENST00000681166.1:n.1435+136_1435+137insC
ENST00000681341.1:n.1529+136_1529+137insC
ENST00000681640.1:n.482+136_482+137insC
ENST00000681948.1:c.643+136_643+137insC	ENSP00000505991.1:n.643+136_643+137insC
ENST00000358971.7:c.*186+136_*186+137insC	ENSP00000351857.3:n.*186+136_*186+137insC
ENST00000382103.6:c.388+136_388+137insC	ENSP00000371535.2:n.388+136_388+137insC
ENST00000514585.5:c.*89+136_*89+137insC	ENSP00000421880.1:n.*89+136_*89+137insC
NM_016955.3:c.388+136_388+137insC	NP_058651.3:n.388+136_388+137insC
XM_005248168.2:c.151+136_151+137insC	XP_005248225.1:n.151+136_151+137insC
XM_006713965.2:c.208+136_208+137insC	XP_006714028.1:n.208+136_208+137insC
XM_011513846.1:c.385+136_385+137insC	XP_011512148.1:n.385+136_385+137insC
XM_011513847.1:c.355+136_355+137insC	XP_011512149.1:n.355+136_355+137insC
XM_011513848.1:c.208+136_208+137insC	XP_011512150.1:n.208+136_208+137insC
XM_011513846.2:c.385+136_385+137insC	XP_011512148.1:n.385+136_385+137insC
XM_011513847.2:c.355+136_355+137insC	XP_011512149.1:n.355+136_355+137insC
XM_017008277.1:c.643+136_643+137insC	XP_016863766.1:n.643+136_643+137insC
XM_017008278.1:c.-36+136_-36+137insC	XP_016863767.1:n.-36+136_-36+137insC
NM_016955.4:c.388+136_388+137insC MANE Select	NP_058651.3:n.388+136_388+137insC