Canonical Allele Identifier: CA1445222839
Gene: SEPSECS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.25144344_25144349delinsAAAGAT , CM000666.2:g.25144344_25144349delinsAAAGAT GRCh38
NC_000004.11:g.25145966_25145971delinsAAAGAT , CM000666.1:g.25145966_25145971delinsAAAGAT GRCh37
NC_000004.10:g.24755064_24755069delinsAAAGAT NCBI36
NG_028222.1:g.21234_21239delinsATCTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000382103.7:c.1026+425_1026+430delinsATCTTT MANE Select ENSP00000371535.2:n.1026+425_1026+430delinsATCTTT
ENST00000680581.1:c.1026+425_1026+430delinsATCTTT ENSP00000506483.1:n.1026+425_1026+430delinsATCTTT
ENST00000680824.1:n.2242+425_2242+430delinsATCTTT
ENST00000681071.1:n.1318+425_1318+430delinsATCTTT
ENST00000681341.1:n.2167+425_2167+430delinsATCTTT
ENST00000681948.1:c.1281+425_1281+430delinsATCTTT ENSP00000505991.1:n.1281+425_1281+430delinsATCTTT
ENST00000358971.7:c.*824+425_*824+430delinsATCTTT ENSP00000351857.3:n.*824+425_*824+430delinsATCTTT
ENST00000382103.6:c.1026+425_1026+430delinsATCTTT ENSP00000371535.2:n.1026+425_1026+430delinsATCTTT
ENST00000503150.1:c.308+425_308+430delinsATCTTT
ENST00000505513.1:n.326+425_326+430delinsATCTTT
ENST00000514585.5:c.*727+425_*727+430delinsATCTTT ENSP00000421880.1:n.*727+425_*727+430delinsATCTTT
NM_016955.3:c.1026+425_1026+430delinsATCTTT NP_058651.3:n.1026+425_1026+430delinsATCTTT
XM_005248168.2:c.789+425_789+430delinsATCTTT XP_005248225.1:n.789+425_789+430delinsATCTTT
XM_006713965.2:c.846+425_846+430delinsATCTTT XP_006714028.1:n.846+425_846+430delinsATCTTT
XM_011513846.1:c.1023+425_1023+430delinsATCTTT XP_011512148.1:n.1023+425_1023+430delinsATCTTT
XM_011513847.1:c.993+425_993+430delinsATCTTT XP_011512149.1:n.993+425_993+430delinsATCTTT
XM_011513848.1:c.846+425_846+430delinsATCTTT XP_011512150.1:n.846+425_846+430delinsATCTTT
XM_011513846.2:c.1023+425_1023+430delinsATCTTT XP_011512148.1:n.1023+425_1023+430delinsATCTTT
XM_011513847.2:c.993+425_993+430delinsATCTTT XP_011512149.1:n.993+425_993+430delinsATCTTT
XM_017008277.1:c.1281+425_1281+430delinsATCTTT XP_016863766.1:n.1281+425_1281+430delinsATCTTT
XM_017008278.1:c.603+425_603+430delinsATCTTT XP_016863767.1:n.603+425_603+430delinsATCTTT
NM_016955.4:c.1026+425_1026+430delinsATCTTT MANE Select NP_058651.3:n.1026+425_1026+430delinsATCTTT