Canonical Allele Identifier: CA1060322874
Gene: SEPSECS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.25144267_25144268insGA , CM000666.2:g.25144267_25144268insGA GRCh38
NC_000004.11:g.25145889_25145890insGA , CM000666.1:g.25145889_25145890insGA GRCh37
NC_000004.10:g.24754987_24754988insGA NCBI36
NG_028222.1:g.21315_21316insTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000382103.7:c.1026+506_1026+507insTC MANE Select ENSP00000371535.2:n.1026+506_1026+507insTC
ENST00000680581.1:c.1026+506_1026+507insTC ENSP00000506483.1:n.1026+506_1026+507insTC
ENST00000680824.1:n.2242+506_2242+507insTC
ENST00000681071.1:n.1318+506_1318+507insTC
ENST00000681341.1:n.2167+506_2167+507insTC
ENST00000681948.1:c.1281+506_1281+507insTC ENSP00000505991.1:n.1281+506_1281+507insTC
ENST00000358971.7:c.*824+506_*824+507insTC ENSP00000351857.3:n.*824+506_*824+507insTC
ENST00000382103.6:c.1026+506_1026+507insTC ENSP00000371535.2:n.1026+506_1026+507insTC
ENST00000503150.1:c.308+506_308+507insTC
ENST00000505513.1:n.326+506_326+507insTC
ENST00000514585.5:c.*727+506_*727+507insTC ENSP00000421880.1:n.*727+506_*727+507insTC
NM_016955.3:c.1026+506_1026+507insTC NP_058651.3:n.1026+506_1026+507insTC
XM_005248168.2:c.789+506_789+507insTC XP_005248225.1:n.789+506_789+507insTC
XM_006713965.2:c.846+506_846+507insTC XP_006714028.1:n.846+506_846+507insTC
XM_011513846.1:c.1023+506_1023+507insTC XP_011512148.1:n.1023+506_1023+507insTC
XM_011513847.1:c.993+506_993+507insTC XP_011512149.1:n.993+506_993+507insTC
XM_011513848.1:c.846+506_846+507insTC XP_011512150.1:n.846+506_846+507insTC
XM_011513846.2:c.1023+506_1023+507insTC XP_011512148.1:n.1023+506_1023+507insTC
XM_011513847.2:c.993+506_993+507insTC XP_011512149.1:n.993+506_993+507insTC
XM_017008277.1:c.1281+506_1281+507insTC XP_016863766.1:n.1281+506_1281+507insTC
XM_017008278.1:c.603+506_603+507insTC XP_016863767.1:n.603+506_603+507insTC
NM_016955.4:c.1026+506_1026+507insTC MANE Select NP_058651.3:n.1026+506_1026+507insTC