Canonical Allele Identifier: CA1445222873
Gene: SEPSECS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.25144355_25144356delinsTA , CM000666.2:g.25144355_25144356delinsTA GRCh38
NC_000004.11:g.25145977_25145978delinsTA , CM000666.1:g.25145977_25145978delinsTA GRCh37
NC_000004.10:g.24755075_24755076delinsTA NCBI36
NG_028222.1:g.21227_21228delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000382103.7:c.1026+418_1026+419delinsTA MANE Select ENSP00000371535.2:n.1026+418_1026+419delinsTA
ENST00000680581.1:c.1026+418_1026+419delinsTA ENSP00000506483.1:n.1026+418_1026+419delinsTA
ENST00000680824.1:n.2242+418_2242+419delinsTA
ENST00000681071.1:n.1318+418_1318+419delinsTA
ENST00000681341.1:n.2167+418_2167+419delinsTA
ENST00000681948.1:c.1281+418_1281+419delinsTA ENSP00000505991.1:n.1281+418_1281+419delinsTA
ENST00000358971.7:c.*824+418_*824+419delinsTA ENSP00000351857.3:n.*824+418_*824+419delinsTA
ENST00000382103.6:c.1026+418_1026+419delinsTA ENSP00000371535.2:n.1026+418_1026+419delinsTA
ENST00000503150.1:c.308+418_308+419delinsTA
ENST00000505513.1:n.326+418_326+419delinsTA
ENST00000514585.5:c.*727+418_*727+419delinsTA ENSP00000421880.1:n.*727+418_*727+419delinsTA
NM_016955.3:c.1026+418_1026+419delinsTA NP_058651.3:n.1026+418_1026+419delinsTA
XM_005248168.2:c.789+418_789+419delinsTA XP_005248225.1:n.789+418_789+419delinsTA
XM_006713965.2:c.846+418_846+419delinsTA XP_006714028.1:n.846+418_846+419delinsTA
XM_011513846.1:c.1023+418_1023+419delinsTA XP_011512148.1:n.1023+418_1023+419delinsTA
XM_011513847.1:c.993+418_993+419delinsTA XP_011512149.1:n.993+418_993+419delinsTA
XM_011513848.1:c.846+418_846+419delinsTA XP_011512150.1:n.846+418_846+419delinsTA
XM_011513846.2:c.1023+418_1023+419delinsTA XP_011512148.1:n.1023+418_1023+419delinsTA
XM_011513847.2:c.993+418_993+419delinsTA XP_011512149.1:n.993+418_993+419delinsTA
XM_017008277.1:c.1281+418_1281+419delinsTA XP_016863766.1:n.1281+418_1281+419delinsTA
XM_017008278.1:c.603+418_603+419delinsTA XP_016863767.1:n.603+418_603+419delinsTA
NM_016955.4:c.1026+418_1026+419delinsTA MANE Select NP_058651.3:n.1026+418_1026+419delinsTA