Canonical Allele Identifier: CA2760775168

Gene: SEPSECS

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156957_25156959del , CM000666.2:g.25156957_25156959del	GRCh38
NC_000004.11:g.25158579_25158581del , CM000666.1:g.25158579_25158581del	GRCh37
NC_000004.10:g.24767677_24767679del	NCBI36
NG_028222.1:g.8624_8626del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.285_287del MANE Select	ENSP00000371535.2:p.Gly96del
ENST00000680581.1:c.285_287del	ENSP00000506483.1:p.Gly96del
ENST00000680824.1:n.1501_1503del
ENST00000681071.1:n.577_579del
ENST00000681166.1:n.1332_1334del
ENST00000681341.1:n.1426_1428del
ENST00000681640.1:n.379_381del
ENST00000681948.1:c.540_542del	ENSP00000505991.1:p.Gly181del
ENST00000358971.7:c.*83_*85del	ENSP00000351857.3:n.*83_*85del
ENST00000382103.6:c.285_287del	ENSP00000371535.2:p.Gly96del
ENST00000514585.5:c.130_132del	ENSP00000421880.1:p.Trp44del
NM_016955.3:c.285_287del	NP_058651.3:p.Gly96del
XM_005248168.2:c.48_50del	XP_005248225.1:p.Gly17del
XM_006713965.2:c.105_107del	XP_006714028.1:p.Gly36del
XM_011513846.1:c.282_284del	XP_011512148.1:p.Gly95del
XM_011513847.1:c.252_254del	XP_011512149.1:p.Gly85del
XM_011513848.1:c.105_107del	XP_011512150.1:p.Gly36del
XM_011513846.2:c.282_284del	XP_011512148.1:p.Gly95del
XM_011513847.2:c.252_254del	XP_011512149.1:p.Gly85del
XM_017008277.1:c.540_542del	XP_016863766.1:p.Gly181del
XM_017008278.1:c.-139_-137del	XP_016863767.1:n.-139_-137del
NM_016955.4:c.285_287del MANE Select	NP_058651.3:p.Gly96del