Canonical Allele Identifier: CA1445207427
Gene: SEPSECS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.25156352_25156353delinsCT , CM000666.2:g.25156352_25156353delinsCT GRCh38
NC_000004.11:g.25157974_25157975delinsCT , CM000666.1:g.25157974_25157975delinsCT GRCh37
NC_000004.10:g.24767072_24767073delinsCT NCBI36
NG_028222.1:g.9230_9231delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000382103.7:c.389-158_389-157delinsAG MANE Select ENSP00000371535.2:n.389-158_389-157delinsAG
ENST00000680581.1:c.389-158_389-157delinsAG ENSP00000506483.1:n.389-158_389-157delinsAG
ENST00000680824.1:n.1605-158_1605-157delinsAG
ENST00000681071.1:n.681-158_681-157delinsAG
ENST00000681166.1:n.1436-158_1436-157delinsAG
ENST00000681341.1:n.1530-158_1530-157delinsAG
ENST00000681640.1:n.483-158_483-157delinsAG
ENST00000681948.1:c.644-158_644-157delinsAG ENSP00000505991.1:n.644-158_644-157delinsAG
ENST00000358971.7:c.*187-158_*187-157delinsAG ENSP00000351857.3:n.*187-158_*187-157delinsAG
ENST00000382103.6:c.389-158_389-157delinsAG ENSP00000371535.2:n.389-158_389-157delinsAG
ENST00000514585.5:c.*90-158_*90-157delinsAG ENSP00000421880.1:n.*90-158_*90-157delinsAG
NM_016955.3:c.389-158_389-157delinsAG NP_058651.3:n.389-158_389-157delinsAG
XM_005248168.2:c.152-158_152-157delinsAG XP_005248225.1:n.152-158_152-157delinsAG
XM_006713965.2:c.209-158_209-157delinsAG XP_006714028.1:n.209-158_209-157delinsAG
XM_011513846.1:c.386-158_386-157delinsAG XP_011512148.1:n.386-158_386-157delinsAG
XM_011513847.1:c.356-158_356-157delinsAG XP_011512149.1:n.356-158_356-157delinsAG
XM_011513848.1:c.209-158_209-157delinsAG XP_011512150.1:n.209-158_209-157delinsAG
XM_011513846.2:c.386-158_386-157delinsAG XP_011512148.1:n.386-158_386-157delinsAG
XM_011513847.2:c.356-158_356-157delinsAG XP_011512149.1:n.356-158_356-157delinsAG
XM_017008277.1:c.644-158_644-157delinsAG XP_016863766.1:n.644-158_644-157delinsAG
XM_017008278.1:c.-35-158_-35-157delinsAG XP_016863767.1:n.-35-158_-35-157delinsAG
NM_016955.4:c.389-158_389-157delinsAG MANE Select NP_058651.3:n.389-158_389-157delinsAG