Canonical Allele Identifier: CA1060322957

Gene: SEPSECS

Linked Data

• dbSNP Id: rs1711819513
• gnomAD v3: 4-25144322-C-CA
• gnomAD v4: 4-25144322-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144322_25144323insA , CM000666.2:g.25144322_25144323insA	GRCh38
NC_000004.11:g.25145944_25145945insA , CM000666.1:g.25145944_25145945insA	GRCh37
NC_000004.10:g.24755042_24755043insA	NCBI36
NG_028222.1:g.21260_21261insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.1026+451_1026+452insT MANE Select	ENSP00000371535.2:n.1026+451_1026+452insT
ENST00000680581.1:c.1026+451_1026+452insT	ENSP00000506483.1:n.1026+451_1026+452insT
ENST00000680824.1:n.2242+451_2242+452insT
ENST00000681071.1:n.1318+451_1318+452insT
ENST00000681341.1:n.2167+451_2167+452insT
ENST00000681948.1:c.1281+451_1281+452insT	ENSP00000505991.1:n.1281+451_1281+452insT
ENST00000358971.7:c.*824+451_*824+452insT	ENSP00000351857.3:n.*824+451_*824+452insT
ENST00000382103.6:c.1026+451_1026+452insT	ENSP00000371535.2:n.1026+451_1026+452insT
ENST00000503150.1:c.308+451_308+452insT
ENST00000505513.1:n.326+451_326+452insT
ENST00000514585.5:c.*727+451_*727+452insT	ENSP00000421880.1:n.*727+451_*727+452insT
NM_016955.3:c.1026+451_1026+452insT	NP_058651.3:n.1026+451_1026+452insT
XM_005248168.2:c.789+451_789+452insT	XP_005248225.1:n.789+451_789+452insT
XM_006713965.2:c.846+451_846+452insT	XP_006714028.1:n.846+451_846+452insT
XM_011513846.1:c.1023+451_1023+452insT	XP_011512148.1:n.1023+451_1023+452insT
XM_011513847.1:c.993+451_993+452insT	XP_011512149.1:n.993+451_993+452insT
XM_011513848.1:c.846+451_846+452insT	XP_011512150.1:n.846+451_846+452insT
XM_011513846.2:c.1023+451_1023+452insT	XP_011512148.1:n.1023+451_1023+452insT
XM_011513847.2:c.993+451_993+452insT	XP_011512149.1:n.993+451_993+452insT
XM_017008277.1:c.1281+451_1281+452insT	XP_016863766.1:n.1281+451_1281+452insT
XM_017008278.1:c.603+451_603+452insT	XP_016863767.1:n.603+451_603+452insT
NM_016955.4:c.1026+451_1026+452insT MANE Select	NP_058651.3:n.1026+451_1026+452insT