Canonical Allele Identifier: CA1445222775

Gene: SEPSECS

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144311_25144312delinsAC , CM000666.2:g.25144311_25144312delinsAC	GRCh38
NC_000004.11:g.25145933_25145934delinsAC , CM000666.1:g.25145933_25145934delinsAC	GRCh37
NC_000004.10:g.24755031_24755032delinsAC	NCBI36
NG_028222.1:g.21271_21272delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.1026+462_1026+463delinsGT MANE Select	ENSP00000371535.2:n.1026+462_1026+463delinsGT
ENST00000680581.1:c.1026+462_1026+463delinsGT	ENSP00000506483.1:n.1026+462_1026+463delinsGT
ENST00000680824.1:n.2242+462_2242+463delinsGT
ENST00000681071.1:n.1318+462_1318+463delinsGT
ENST00000681341.1:n.2167+462_2167+463delinsGT
ENST00000681948.1:c.1281+462_1281+463delinsGT	ENSP00000505991.1:n.1281+462_1281+463delinsGT
ENST00000358971.7:c.*824+462_*824+463delinsGT	ENSP00000351857.3:n.*824+462_*824+463delinsGT
ENST00000382103.6:c.1026+462_1026+463delinsGT	ENSP00000371535.2:n.1026+462_1026+463delinsGT
ENST00000503150.1:c.308+462_308+463delinsGT
ENST00000505513.1:n.326+462_326+463delinsGT
ENST00000514585.5:c.*727+462_*727+463delinsGT	ENSP00000421880.1:n.*727+462_*727+463delinsGT
NM_016955.3:c.1026+462_1026+463delinsGT	NP_058651.3:n.1026+462_1026+463delinsGT
XM_005248168.2:c.789+462_789+463delinsGT	XP_005248225.1:n.789+462_789+463delinsGT
XM_006713965.2:c.846+462_846+463delinsGT	XP_006714028.1:n.846+462_846+463delinsGT
XM_011513846.1:c.1023+462_1023+463delinsGT	XP_011512148.1:n.1023+462_1023+463delinsGT
XM_011513847.1:c.993+462_993+463delinsGT	XP_011512149.1:n.993+462_993+463delinsGT
XM_011513848.1:c.846+462_846+463delinsGT	XP_011512150.1:n.846+462_846+463delinsGT
XM_011513846.2:c.1023+462_1023+463delinsGT	XP_011512148.1:n.1023+462_1023+463delinsGT
XM_011513847.2:c.993+462_993+463delinsGT	XP_011512149.1:n.993+462_993+463delinsGT
XM_017008277.1:c.1281+462_1281+463delinsGT	XP_016863766.1:n.1281+462_1281+463delinsGT
XM_017008278.1:c.603+462_603+463delinsGT	XP_016863767.1:n.603+462_603+463delinsGT
NM_016955.4:c.1026+462_1026+463delinsGT MANE Select	NP_058651.3:n.1026+462_1026+463delinsGT