Canonical Allele Identifier: CA1445208887
Gene: SEPSECS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.25156976_25156983delinsTAAGCAAA , CM000666.2:g.25156976_25156983delinsTAAGCAAA GRCh38
NC_000004.11:g.25158598_25158605delinsTAAGCAAA , CM000666.1:g.25158598_25158605delinsTAAGCAAA GRCh37
NC_000004.10:g.24767696_24767703delinsTAAGCAAA NCBI36
NG_028222.1:g.8600_8607delinsTTTGCTTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000382103.7:c.270-9_270-2delinsTTTGCTTA MANE Select ENSP00000371535.2:n.270-9_270-2delinsTTTGCTTA
ENST00000680581.1:c.270-9_270-2delinsTTTGCTTA ENSP00000506483.1:n.270-9_270-2delinsTTTGCTTA
ENST00000680824.1:n.1486-9_1486-2delinsTTTGCTTA
ENST00000681071.1:n.553_560delinsTTTGCTTA
ENST00000681166.1:n.1317-9_1317-2delinsTTTGCTTA
ENST00000681341.1:n.1411-9_1411-2delinsTTTGCTTA
ENST00000681640.1:n.364-9_364-2delinsTTTGCTTA
ENST00000681948.1:c.525-9_525-2delinsTTTGCTTA ENSP00000505991.1:n.525-9_525-2delinsTTTGCTTA
ENST00000358971.7:c.*68-9_*68-2delinsTTTGCTTA ENSP00000351857.3:n.*68-9_*68-2delinsTTTGCTTA
ENST00000382103.6:c.270-9_270-2delinsTTTGCTTA ENSP00000371535.2:n.270-9_270-2delinsTTTGCTTA
ENST00000514585.5:c.115-9_115-2delinsTTTGCTTA ENSP00000421880.1:n.115-9_115-2delinsTTTGCTTA
NM_016955.3:c.270-9_270-2delinsTTTGCTTA NP_058651.3:n.270-9_270-2delinsTTTGCTTA
XM_005248168.2:c.33-9_33-2delinsTTTGCTTA XP_005248225.1:n.33-9_33-2delinsTTTGCTTA
XM_006713965.2:c.90-9_90-2delinsTTTGCTTA XP_006714028.1:n.90-9_90-2delinsTTTGCTTA
XM_011513846.1:c.267-9_267-2delinsTTTGCTTA XP_011512148.1:n.267-9_267-2delinsTTTGCTTA
XM_011513847.1:c.237-9_237-2delinsTTTGCTTA XP_011512149.1:n.237-9_237-2delinsTTTGCTTA
XM_011513848.1:c.90-9_90-2delinsTTTGCTTA XP_011512150.1:n.90-9_90-2delinsTTTGCTTA
XM_011513846.2:c.267-9_267-2delinsTTTGCTTA XP_011512148.1:n.267-9_267-2delinsTTTGCTTA
XM_011513847.2:c.237-9_237-2delinsTTTGCTTA XP_011512149.1:n.237-9_237-2delinsTTTGCTTA
XM_017008277.1:c.525-9_525-2delinsTTTGCTTA XP_016863766.1:n.525-9_525-2delinsTTTGCTTA
XM_017008278.1:c.-163_-156delinsTTTGCTTA XP_016863767.1:n.-163_-156delinsTTTGCTTA
NM_016955.4:c.270-9_270-2delinsTTTGCTTA MANE Select NP_058651.3:n.270-9_270-2delinsTTTGCTTA