Canonical Allele Identifier: CA2535559593
Gene: SEPSECS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.25144541_25144542insACAAATGGATAAGTCATCTTTT , CM000666.2:g.25144541_25144542insACAAATGGATAAGTCATCTTTT GRCh38
NC_000004.11:g.25146163_25146164insACAAATGGATAAGTCATCTTTT , CM000666.1:g.25146163_25146164insACAAATGGATAAGTCATCTTTT GRCh37
NC_000004.10:g.24755261_24755262insACAAATGGATAAGTCATCTTTT NCBI36
NG_028222.1:g.21041_21042insAAAAGATGACTTATCCATTTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000382103.7:c.1026+232_1026+233insAAAAGATGACTTATCCATTTGT MANE Select ENSP00000371535.2:n.1026+232_1026+233insAAAAGATGACTTATCCATTTG...
ENST00000680581.1:c.1026+232_1026+233insAAAAGATGACTTATCCATTTGT ENSP00000506483.1:n.1026+232_1026+233insAAAAGATGACTTATCCATTTG...
ENST00000680824.1:n.2242+232_2242+233insAAAAGATGACTTATCCATTTGT
ENST00000681071.1:n.1318+232_1318+233insAAAAGATGACTTATCCATTTGT
ENST00000681341.1:n.2167+232_2167+233insAAAAGATGACTTATCCATTTGT
ENST00000681948.1:c.1281+232_1281+233insAAAAGATGACTTATCCATTTGT ENSP00000505991.1:n.1281+232_1281+233insAAAAGATGACTTATCCATTTG...
ENST00000358971.7:c.*824+232_*824+233insAAAAGATGACTTATCCATTTGT ENSP00000351857.3:n.*824+232_*824+233insAAAAGATGACTTATCCATTTG...
ENST00000382103.6:c.1026+232_1026+233insAAAAGATGACTTATCCATTTGT ENSP00000371535.2:n.1026+232_1026+233insAAAAGATGACTTATCCATTTG...
ENST00000503150.1:c.308+232_308+233insAAAAGATGACTTATCCATTTGT
ENST00000505513.1:n.326+232_326+233insAAAAGATGACTTATCCATTTGT
ENST00000514585.5:c.*727+232_*727+233insAAAAGATGACTTATCCATTTGT ENSP00000421880.1:n.*727+232_*727+233insAAAAGATGACTTATCCATTTG...
NM_016955.3:c.1026+232_1026+233insAAAAGATGACTTATCCATTTGT NP_058651.3:n.1026+232_1026+233insAAAAGATGACTTATCCATTTGT
XM_005248168.2:c.789+232_789+233insAAAAGATGACTTATCCATTTGT XP_005248225.1:n.789+232_789+233insAAAAGATGACTTATCCATTTGT
XM_006713965.2:c.846+232_846+233insAAAAGATGACTTATCCATTTGT XP_006714028.1:n.846+232_846+233insAAAAGATGACTTATCCATTTGT
XM_011513846.1:c.1023+232_1023+233insAAAAGATGACTTATCCATTTGT XP_011512148.1:n.1023+232_1023+233insAAAAGATGACTTATCCATTTGT
XM_011513847.1:c.993+232_993+233insAAAAGATGACTTATCCATTTGT XP_011512149.1:n.993+232_993+233insAAAAGATGACTTATCCATTTGT
XM_011513848.1:c.846+232_846+233insAAAAGATGACTTATCCATTTGT XP_011512150.1:n.846+232_846+233insAAAAGATGACTTATCCATTTGT
XM_011513846.2:c.1023+232_1023+233insAAAAGATGACTTATCCATTTGT XP_011512148.1:n.1023+232_1023+233insAAAAGATGACTTATCCATTTGT
XM_011513847.2:c.993+232_993+233insAAAAGATGACTTATCCATTTGT XP_011512149.1:n.993+232_993+233insAAAAGATGACTTATCCATTTGT
XM_017008277.1:c.1281+232_1281+233insAAAAGATGACTTATCCATTTGT XP_016863766.1:n.1281+232_1281+233insAAAAGATGACTTATCCATTTGT
XM_017008278.1:c.603+232_603+233insAAAAGATGACTTATCCATTTGT XP_016863767.1:n.603+232_603+233insAAAAGATGACTTATCCATTTGT
NM_016955.4:c.1026+232_1026+233insAAAAGATGACTTATCCATTTGT MANE Select NP_058651.3:n.1026+232_1026+233insAAAAGATGACTTATCCATTTGT