Canonical Allele Identifier: CA1445208465

Gene: SEPSECS

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156735_25156746delinsAGAAGTCTTTTC , CM000666.2:g.25156735_25156746delinsAGAAGTCTTTTC	GRCh38
NC_000004.11:g.25158357_25158368delinsAGAAGTCTTTTC , CM000666.1:g.25158357_25158368delinsAGAAGTCTTTTC	GRCh37
NC_000004.10:g.24767455_24767466delinsAGAAGTCTTTTC	NCBI36
NG_028222.1:g.8837_8848delinsGAAAAGACTTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.388+110_388+121delinsGAAAAGACTTCT MANE Select	ENSP00000371535.2:n.388+110_388+121delinsGAAAAGACTTCT
ENST00000680581.1:c.388+110_388+121delinsGAAAAGACTTCT	ENSP00000506483.1:n.388+110_388+121delinsGAAAAGACTTCT
ENST00000680824.1:n.1604+110_1604+121delinsGAAAAGACTTCT
ENST00000681071.1:n.680+110_680+121delinsGAAAAGACTTCT
ENST00000681166.1:n.1435+110_1435+121delinsGAAAAGACTTCT
ENST00000681341.1:n.1529+110_1529+121delinsGAAAAGACTTCT
ENST00000681640.1:n.482+110_482+121delinsGAAAAGACTTCT
ENST00000681948.1:c.643+110_643+121delinsGAAAAGACTTCT	ENSP00000505991.1:n.643+110_643+121delinsGAAAAGACTTCT
ENST00000358971.7:c.*186+110_*186+121delinsGAAAAGACTTCT	ENSP00000351857.3:n.*186+110_*186+121delinsGAAAAGACTTCT
ENST00000382103.6:c.388+110_388+121delinsGAAAAGACTTCT	ENSP00000371535.2:n.388+110_388+121delinsGAAAAGACTTCT
ENST00000514585.5:c.*89+110_*89+121delinsGAAAAGACTTCT	ENSP00000421880.1:n.*89+110_*89+121delinsGAAAAGACTTCT
NM_016955.3:c.388+110_388+121delinsGAAAAGACTTCT	NP_058651.3:n.388+110_388+121delinsGAAAAGACTTCT
XM_005248168.2:c.151+110_151+121delinsGAAAAGACTTCT	XP_005248225.1:n.151+110_151+121delinsGAAAAGACTTCT
XM_006713965.2:c.208+110_208+121delinsGAAAAGACTTCT	XP_006714028.1:n.208+110_208+121delinsGAAAAGACTTCT
XM_011513846.1:c.385+110_385+121delinsGAAAAGACTTCT	XP_011512148.1:n.385+110_385+121delinsGAAAAGACTTCT
XM_011513847.1:c.355+110_355+121delinsGAAAAGACTTCT	XP_011512149.1:n.355+110_355+121delinsGAAAAGACTTCT
XM_011513848.1:c.208+110_208+121delinsGAAAAGACTTCT	XP_011512150.1:n.208+110_208+121delinsGAAAAGACTTCT
XM_011513846.2:c.385+110_385+121delinsGAAAAGACTTCT	XP_011512148.1:n.385+110_385+121delinsGAAAAGACTTCT
XM_011513847.2:c.355+110_355+121delinsGAAAAGACTTCT	XP_011512149.1:n.355+110_355+121delinsGAAAAGACTTCT
XM_017008277.1:c.643+110_643+121delinsGAAAAGACTTCT	XP_016863766.1:n.643+110_643+121delinsGAAAAGACTTCT
XM_017008278.1:c.-36+110_-36+121delinsGAAAAGACTTCT	XP_016863767.1:n.-36+110_-36+121delinsGAAAAGACTTCT
NM_016955.4:c.388+110_388+121delinsGAAAAGACTTCT MANE Select	NP_058651.3:n.388+110_388+121delinsGAAAAGACTTCT