Canonical Allele Identifier: CA2538262559

Gene: SEPSECS

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144326_25144327insT , CM000666.2:g.25144326_25144327insT	GRCh38
NC_000004.11:g.25145948_25145949insT , CM000666.1:g.25145948_25145949insT	GRCh37
NC_000004.10:g.24755046_24755047insT	NCBI36
NG_028222.1:g.21256_21257insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.1026+447_1026+448insA MANE Select	ENSP00000371535.2:n.1026+447_1026+448insA
ENST00000680581.1:c.1026+447_1026+448insA	ENSP00000506483.1:n.1026+447_1026+448insA
ENST00000680824.1:n.2242+447_2242+448insA
ENST00000681071.1:n.1318+447_1318+448insA
ENST00000681341.1:n.2167+447_2167+448insA
ENST00000681948.1:c.1281+447_1281+448insA	ENSP00000505991.1:n.1281+447_1281+448insA
ENST00000358971.7:c.*824+447_*824+448insA	ENSP00000351857.3:n.*824+447_*824+448insA
ENST00000382103.6:c.1026+447_1026+448insA	ENSP00000371535.2:n.1026+447_1026+448insA
ENST00000503150.1:c.308+447_308+448insA
ENST00000505513.1:n.326+447_326+448insA
ENST00000514585.5:c.*727+447_*727+448insA	ENSP00000421880.1:n.*727+447_*727+448insA
NM_016955.3:c.1026+447_1026+448insA	NP_058651.3:n.1026+447_1026+448insA
XM_005248168.2:c.789+447_789+448insA	XP_005248225.1:n.789+447_789+448insA
XM_006713965.2:c.846+447_846+448insA	XP_006714028.1:n.846+447_846+448insA
XM_011513846.1:c.1023+447_1023+448insA	XP_011512148.1:n.1023+447_1023+448insA
XM_011513847.1:c.993+447_993+448insA	XP_011512149.1:n.993+447_993+448insA
XM_011513848.1:c.846+447_846+448insA	XP_011512150.1:n.846+447_846+448insA
XM_011513846.2:c.1023+447_1023+448insA	XP_011512148.1:n.1023+447_1023+448insA
XM_011513847.2:c.993+447_993+448insA	XP_011512149.1:n.993+447_993+448insA
XM_017008277.1:c.1281+447_1281+448insA	XP_016863766.1:n.1281+447_1281+448insA
XM_017008278.1:c.603+447_603+448insA	XP_016863767.1:n.603+447_603+448insA
NM_016955.4:c.1026+447_1026+448insA MANE Select	NP_058651.3:n.1026+447_1026+448insA