Canonical Allele Identifier: CA2594465696
Gene: SEPSECS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.25144346_25144347insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA , CM000666.2:g.25144346_25144347insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA GRCh38
NC_000004.11:g.25145968_25145969insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA , CM000666.1:g.25145968_25145969insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA GRCh37
NC_000004.10:g.24755066_24755067insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA NCBI36
NG_028222.1:g.21256_21257insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000382103.7:c.1026+447_1026+448insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT MANE Select ENSP00000371535.2:n.1026+447_1026+448insTTTTTTTTTTTTTTTTTTTTT...
ENST00000680581.1:c.1026+447_1026+448insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000506483.1:n.1026+447_1026+448insTTTTTTTTTTTTTTTTTTTTT...
ENST00000680824.1:n.2242+447_2242+448insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000681071.1:n.1318+447_1318+448insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000681341.1:n.2167+447_2167+448insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000681948.1:c.1281+447_1281+448insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000505991.1:n.1281+447_1281+448insTTTTTTTTTTTTTTTTTTTTT...
ENST00000358971.7:c.*824+447_*824+448insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000351857.3:n.*824+447_*824+448insTTTTTTTTTTTTTTTTTTTTT...
ENST00000382103.6:c.1026+447_1026+448insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000371535.2:n.1026+447_1026+448insTTTTTTTTTTTTTTTTTTTTT...
ENST00000503150.1:c.308+447_308+448insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000505513.1:n.326+447_326+448insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000514585.5:c.*727+447_*727+448insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000421880.1:n.*727+447_*727+448insTTTTTTTTTTTTTTTTTTTTT...
NM_016955.3:c.1026+447_1026+448insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NP_058651.3:n.1026+447_1026+448insTTTTTTTTTTTTTTTTTTTTTTTTTTT...
XM_005248168.2:c.789+447_789+448insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_005248225.1:n.789+447_789+448insTTTTTTTTTTTTTTTTTTTTTTTTTT...
XM_006713965.2:c.846+447_846+448insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_006714028.1:n.846+447_846+448insTTTTTTTTTTTTTTTTTTTTTTTTTT...
XM_011513846.1:c.1023+447_1023+448insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_011512148.1:n.1023+447_1023+448insTTTTTTTTTTTTTTTTTTTTTTTT...
XM_011513847.1:c.993+447_993+448insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_011512149.1:n.993+447_993+448insTTTTTTTTTTTTTTTTTTTTTTTTTT...
XM_011513848.1:c.846+447_846+448insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_011512150.1:n.846+447_846+448insTTTTTTTTTTTTTTTTTTTTTTTTTT...
XM_011513846.2:c.1023+447_1023+448insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_011512148.1:n.1023+447_1023+448insTTTTTTTTTTTTTTTTTTTTTTTT...
XM_011513847.2:c.993+447_993+448insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_011512149.1:n.993+447_993+448insTTTTTTTTTTTTTTTTTTTTTTTTTT...
XM_017008277.1:c.1281+447_1281+448insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_016863766.1:n.1281+447_1281+448insTTTTTTTTTTTTTTTTTTTTTTTT...
XM_017008278.1:c.603+447_603+448insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_016863767.1:n.603+447_603+448insTTTTTTTTTTTTTTTTTTTTTTTTTT...
NM_016955.4:c.1026+447_1026+448insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT MANE Select NP_058651.3:n.1026+447_1026+448insTTTTTTTTTTTTTTTTTTTTTTTTTTT...