Canonical Allele Identifier: CA1445204390
Gene: SEPSECS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.25120813_25120814delinsGA , CM000666.2:g.25120813_25120814delinsGA GRCh38
NC_000004.11:g.25122435_25122436delinsGA , CM000666.1:g.25122435_25122436delinsGA GRCh37
NC_000004.10:g.24731533_24731534delinsGA NCBI36
NG_028222.1:g.44769_44770delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000382103.7:c.*3117_*3118delinsTC MANE Select ENSP00000371535.2:n.*3117_*3118delinsTC
ENST00000680581.1:c.*3497_*3498delinsTC ENSP00000506483.1:n.*3497_*3498delinsTC
ENST00000680824.1:n.5839_5840delinsTC
ENST00000681071.1:n.4915_4916delinsTC
ENST00000681341.1:n.5670_5671delinsTC
ENST00000681374.1:n.3979_3980delinsTC
ENST00000681948.1:c.*3117_*3118delinsTC ENSP00000505991.1:n.*3117_*3118delinsTC
ENST00000382103.6:c.*3117_*3118delinsTC ENSP00000371535.2:n.*3117_*3118delinsTC
NM_016955.3:c.*3117_*3118delinsTC NP_058651.3:n.*3117_*3118delinsTC
XM_005248168.2:c.*3117_*3118delinsTC XP_005248225.1:n.*3117_*3118delinsTC
XM_006713965.2:c.*3117_*3118delinsTC XP_006714028.1:n.*3117_*3118delinsTC
XM_011513846.1:c.*3117_*3118delinsTC XP_011512148.1:n.*3117_*3118delinsTC
XM_011513847.1:c.*3117_*3118delinsTC XP_011512149.1:n.*3117_*3118delinsTC
XM_011513848.1:c.*3117_*3118delinsTC XP_011512150.1:n.*3117_*3118delinsTC
XM_011513846.2:c.*3117_*3118delinsTC XP_011512148.1:n.*3117_*3118delinsTC
XM_011513847.2:c.*3117_*3118delinsTC XP_011512149.1:n.*3117_*3118delinsTC
XM_017008277.1:c.*3117_*3118delinsTC XP_016863766.1:n.*3117_*3118delinsTC
XM_017008278.1:c.*3117_*3118delinsTC XP_016863767.1:n.*3117_*3118delinsTC
NM_016955.4:c.*3117_*3118delinsTC MANE Select NP_058651.3:n.*3117_*3118delinsTC