Canonical Allele Identifier: CA93607507

Gene: SEPSECS

Linked Data

• dbSNP Id: rs777130834
• MyVariant Identifiers: chr4:g.25122492_25122493del (hg19) ; chr4:g.25120870_25120871del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25120873_25120874del , CM000666.2:g.25120873_25120874del	GRCh38
NC_000004.11:g.25122495_25122496del , CM000666.1:g.25122495_25122496del	GRCh37
NC_000004.10:g.24731593_24731594del	NCBI36
NG_028222.1:g.44712_44713del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.*3060_*3061del MANE Select	ENSP00000371535.2:n.*3060_*3061del
ENST00000680581.1:c.*3440_*3441del	ENSP00000506483.1:n.*3440_*3441del
ENST00000680824.1:n.5782_5783del
ENST00000681071.1:n.4858_4859del
ENST00000681341.1:n.5613_5614del
ENST00000681374.1:n.3922_3923del
ENST00000681948.1:c.*3060_*3061del	ENSP00000505991.1:n.*3060_*3061del
ENST00000382103.6:c.*3060_*3061del	ENSP00000371535.2:n.*3060_*3061del
NM_016955.3:c.*3060_*3061del	NP_058651.3:n.*3060_*3061del
XM_005248168.2:c.*3060_*3061del	XP_005248225.1:n.*3060_*3061del
XM_006713965.2:c.*3060_*3061del	XP_006714028.1:n.*3060_*3061del
XM_011513846.1:c.*3060_*3061del	XP_011512148.1:n.*3060_*3061del
XM_011513847.1:c.*3060_*3061del	XP_011512149.1:n.*3060_*3061del
XM_011513848.1:c.*3060_*3061del	XP_011512150.1:n.*3060_*3061del
XM_011513846.2:c.*3060_*3061del	XP_011512148.1:n.*3060_*3061del
XM_011513847.2:c.*3060_*3061del	XP_011512149.1:n.*3060_*3061del
XM_017008277.1:c.*3060_*3061del	XP_016863766.1:n.*3060_*3061del
XM_017008278.1:c.*3060_*3061del	XP_016863767.1:n.*3060_*3061del
NM_016955.4:c.*3060_*3061del MANE Select	NP_058651.3:n.*3060_*3061del