Canonical Allele Identifier: CA2670196412

Gene: SEPSECS

Linked Data

• gnomAD v4: 4-25144632-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144634del , CM000666.2:g.25144634del	GRCh38
NC_000004.11:g.25146256del , CM000666.1:g.25146256del	GRCh37
NC_000004.10:g.24755354del	NCBI36
NG_028222.1:g.20950del

Transcript Alleles

HGVS	Amino-acid change
ENST00000382103.7:c.1026+141del MANE Select	ENSP00000371535.2:n.1026+141del
ENST00000680581.1:c.1026+141del	ENSP00000506483.1:n.1026+141del
ENST00000680824.1:n.2242+141del
ENST00000681071.1:n.1318+141del
ENST00000681341.1:n.2167+141del
ENST00000681948.1:c.1281+141del	ENSP00000505991.1:n.1281+141del
ENST00000358971.7:c.*824+141del	ENSP00000351857.3:n.*824+141del
ENST00000382103.6:c.1026+141del	ENSP00000371535.2:n.1026+141del
ENST00000503150.1:c.308+141del
ENST00000505513.1:n.326+141del
ENST00000514585.5:c.*727+141del	ENSP00000421880.1:n.*727+141del
NM_016955.3:c.1026+141del	NP_058651.3:n.1026+141del
XM_005248168.2:c.789+141del	XP_005248225.1:n.789+141del
XM_006713965.2:c.846+141del	XP_006714028.1:n.846+141del
XM_011513846.1:c.1023+141del	XP_011512148.1:n.1023+141del
XM_011513847.1:c.993+141del	XP_011512149.1:n.993+141del
XM_011513848.1:c.846+141del	XP_011512150.1:n.846+141del
XM_011513846.2:c.1023+141del	XP_011512148.1:n.1023+141del
XM_011513847.2:c.993+141del	XP_011512149.1:n.993+141del
XM_017008277.1:c.1281+141del	XP_016863766.1:n.1281+141del
XM_017008278.1:c.603+141del	XP_016863767.1:n.603+141del
NM_016955.4:c.1026+141del MANE Select	NP_058651.3:n.1026+141del