Canonical Allele Identifier: CA2670196741

Gene: SEPSECS

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25145134del , CM000666.2:g.25145134del	GRCh38
NC_000004.11:g.25146756del , CM000666.1:g.25146756del	GRCh37
NC_000004.10:g.24755854del	NCBI36
NG_028222.1:g.20453del

Transcript Alleles

HGVS	Amino-acid Change
NM_016955.3:c.808del
NM_016955.4:c.808del
ENST00000358971.7:c.*606del
ENST00000382103.6:c.808del
ENST00000382103.7:c.808del
ENST00000503150.1:c.217-265del
ENST00000505513.1:n.235-265del
ENST00000514585.5:c.*509del
ENST00000680581.1:c.808del
ENST00000680824.1:n.2024del
ENST00000681071.1:n.1100del
ENST00000681341.1:n.1949del
ENST00000681948.1:c.1063del
XM_005248168.2:c.571del
XM_006713965.2:c.628del
XM_011513846.1:c.805del
XM_011513846.2:c.805del
XM_011513847.1:c.775del
XM_011513847.2:c.775del
XM_011513848.1:c.628del
XM_017008277.1:c.1063del
XM_017008278.1:c.385del