Canonical Allele Identifier: CA2528278061
Gene: SEPSECS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.25144313_25144314insTGGG , CM000666.2:g.25144313_25144314insTGGG GRCh38
NC_000004.11:g.25145935_25145936insTGGG , CM000666.1:g.25145935_25145936insTGGG GRCh37
NC_000004.10:g.24755033_24755034insTGGG NCBI36
NG_028222.1:g.21269_21270insCCCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000382103.7:c.1026+460_1026+461insCCCA MANE Select ENSP00000371535.2:n.1026+460_1026+461insCCCA
ENST00000680581.1:c.1026+460_1026+461insCCCA ENSP00000506483.1:n.1026+460_1026+461insCCCA
ENST00000680824.1:n.2242+460_2242+461insCCCA
ENST00000681071.1:n.1318+460_1318+461insCCCA
ENST00000681341.1:n.2167+460_2167+461insCCCA
ENST00000681948.1:c.1281+460_1281+461insCCCA ENSP00000505991.1:n.1281+460_1281+461insCCCA
ENST00000358971.7:c.*824+460_*824+461insCCCA ENSP00000351857.3:n.*824+460_*824+461insCCCA
ENST00000382103.6:c.1026+460_1026+461insCCCA ENSP00000371535.2:n.1026+460_1026+461insCCCA
ENST00000503150.1:c.308+460_308+461insCCCA
ENST00000505513.1:n.326+460_326+461insCCCA
ENST00000514585.5:c.*727+460_*727+461insCCCA ENSP00000421880.1:n.*727+460_*727+461insCCCA
NM_016955.3:c.1026+460_1026+461insCCCA NP_058651.3:n.1026+460_1026+461insCCCA
XM_005248168.2:c.789+460_789+461insCCCA XP_005248225.1:n.789+460_789+461insCCCA
XM_006713965.2:c.846+460_846+461insCCCA XP_006714028.1:n.846+460_846+461insCCCA
XM_011513846.1:c.1023+460_1023+461insCCCA XP_011512148.1:n.1023+460_1023+461insCCCA
XM_011513847.1:c.993+460_993+461insCCCA XP_011512149.1:n.993+460_993+461insCCCA
XM_011513848.1:c.846+460_846+461insCCCA XP_011512150.1:n.846+460_846+461insCCCA
XM_011513846.2:c.1023+460_1023+461insCCCA XP_011512148.1:n.1023+460_1023+461insCCCA
XM_011513847.2:c.993+460_993+461insCCCA XP_011512149.1:n.993+460_993+461insCCCA
XM_017008277.1:c.1281+460_1281+461insCCCA XP_016863766.1:n.1281+460_1281+461insCCCA
XM_017008278.1:c.603+460_603+461insCCCA XP_016863767.1:n.603+460_603+461insCCCA
NM_016955.4:c.1026+460_1026+461insCCCA MANE Select NP_058651.3:n.1026+460_1026+461insCCCA