Canonical Allele Identifier: CA1445222889

Gene: SEPSECS

Linked Data

• dbSNP Id: rs1711829437

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144374_25144375dup , CM000666.2:g.25144374_25144375dup	GRCh38
NC_000004.11:g.25145996_25145997dup , CM000666.1:g.25145996_25145997dup	GRCh37
NC_000004.10:g.24755094_24755095dup	NCBI36
NG_028222.1:g.21208_21209dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.1026+399_1026+400dup MANE Select	ENSP00000371535.2:n.1026+399_1026+400dup
ENST00000680581.1:c.1026+399_1026+400dup	ENSP00000506483.1:n.1026+399_1026+400dup
ENST00000680824.1:n.2242+399_2242+400dup
ENST00000681071.1:n.1318+399_1318+400dup
ENST00000681341.1:n.2167+399_2167+400dup
ENST00000681948.1:c.1281+399_1281+400dup	ENSP00000505991.1:n.1281+399_1281+400dup
ENST00000358971.7:c.*824+399_*824+400dup	ENSP00000351857.3:n.*824+399_*824+400dup
ENST00000382103.6:c.1026+399_1026+400dup	ENSP00000371535.2:n.1026+399_1026+400dup
ENST00000503150.1:c.308+399_308+400dup
ENST00000505513.1:n.326+399_326+400dup
ENST00000514585.5:c.*727+399_*727+400dup	ENSP00000421880.1:n.*727+399_*727+400dup
NM_016955.3:c.1026+399_1026+400dup	NP_058651.3:n.1026+399_1026+400dup
XM_005248168.2:c.789+399_789+400dup	XP_005248225.1:n.789+399_789+400dup
XM_006713965.2:c.846+399_846+400dup	XP_006714028.1:n.846+399_846+400dup
XM_011513846.1:c.1023+399_1023+400dup	XP_011512148.1:n.1023+399_1023+400dup
XM_011513847.1:c.993+399_993+400dup	XP_011512149.1:n.993+399_993+400dup
XM_011513848.1:c.846+399_846+400dup	XP_011512150.1:n.846+399_846+400dup
XM_011513846.2:c.1023+399_1023+400dup	XP_011512148.1:n.1023+399_1023+400dup
XM_011513847.2:c.993+399_993+400dup	XP_011512149.1:n.993+399_993+400dup
XM_017008277.1:c.1281+399_1281+400dup	XP_016863766.1:n.1281+399_1281+400dup
XM_017008278.1:c.603+399_603+400dup	XP_016863767.1:n.603+399_603+400dup
NM_016955.4:c.1026+399_1026+400dup MANE Select	NP_058651.3:n.1026+399_1026+400dup