Canonical Allele Identifier: CA1445223011
Gene: SEPSECS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.25144535_25144536delinsTA , CM000666.2:g.25144535_25144536delinsTA GRCh38
NC_000004.11:g.25146157_25146158delinsTA , CM000666.1:g.25146157_25146158delinsTA GRCh37
NC_000004.10:g.24755255_24755256delinsTA NCBI36
NG_028222.1:g.21047_21048delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000382103.7:c.1026+238_1026+239delinsTA MANE Select ENSP00000371535.2:n.1026+238_1026+239delinsTA
ENST00000680581.1:c.1026+238_1026+239delinsTA ENSP00000506483.1:n.1026+238_1026+239delinsTA
ENST00000680824.1:n.2242+238_2242+239delinsTA
ENST00000681071.1:n.1318+238_1318+239delinsTA
ENST00000681341.1:n.2167+238_2167+239delinsTA
ENST00000681948.1:c.1281+238_1281+239delinsTA ENSP00000505991.1:n.1281+238_1281+239delinsTA
ENST00000358971.7:c.*824+238_*824+239delinsTA ENSP00000351857.3:n.*824+238_*824+239delinsTA
ENST00000382103.6:c.1026+238_1026+239delinsTA ENSP00000371535.2:n.1026+238_1026+239delinsTA
ENST00000503150.1:c.308+238_308+239delinsTA
ENST00000505513.1:n.326+238_326+239delinsTA
ENST00000514585.5:c.*727+238_*727+239delinsTA ENSP00000421880.1:n.*727+238_*727+239delinsTA
NM_016955.3:c.1026+238_1026+239delinsTA NP_058651.3:n.1026+238_1026+239delinsTA
XM_005248168.2:c.789+238_789+239delinsTA XP_005248225.1:n.789+238_789+239delinsTA
XM_006713965.2:c.846+238_846+239delinsTA XP_006714028.1:n.846+238_846+239delinsTA
XM_011513846.1:c.1023+238_1023+239delinsTA XP_011512148.1:n.1023+238_1023+239delinsTA
XM_011513847.1:c.993+238_993+239delinsTA XP_011512149.1:n.993+238_993+239delinsTA
XM_011513848.1:c.846+238_846+239delinsTA XP_011512150.1:n.846+238_846+239delinsTA
XM_011513846.2:c.1023+238_1023+239delinsTA XP_011512148.1:n.1023+238_1023+239delinsTA
XM_011513847.2:c.993+238_993+239delinsTA XP_011512149.1:n.993+238_993+239delinsTA
XM_017008277.1:c.1281+238_1281+239delinsTA XP_016863766.1:n.1281+238_1281+239delinsTA
XM_017008278.1:c.603+238_603+239delinsTA XP_016863767.1:n.603+238_603+239delinsTA
NM_016955.4:c.1026+238_1026+239delinsTA MANE Select NP_058651.3:n.1026+238_1026+239delinsTA