Canonical Allele Identifier: CA1445204434

Gene: SEPSECS

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25120879_25120881delinsATC , CM000666.2:g.25120879_25120881delinsATC	GRCh38
NC_000004.11:g.25122501_25122503delinsATC , CM000666.1:g.25122501_25122503delinsATC	GRCh37
NC_000004.10:g.24731599_24731601delinsATC	NCBI36
NG_028222.1:g.44702_44704delinsGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.*3050_*3052delinsGAT MANE Select	ENSP00000371535.2:n.*3050_*3052delinsGAT
ENST00000680581.1:c.*3430_*3432delinsGAT	ENSP00000506483.1:n.*3430_*3432delinsGAT
ENST00000680824.1:n.5772_5774delinsGAT
ENST00000681071.1:n.4848_4850delinsGAT
ENST00000681341.1:n.5603_5605delinsGAT
ENST00000681374.1:n.3912_3914delinsGAT
ENST00000681948.1:c.*3050_*3052delinsGAT	ENSP00000505991.1:n.*3050_*3052delinsGAT
ENST00000382103.6:c.*3050_*3052delinsGAT	ENSP00000371535.2:n.*3050_*3052delinsGAT
NM_016955.3:c.*3050_*3052delinsGAT	NP_058651.3:n.*3050_*3052delinsGAT
XM_005248168.2:c.*3050_*3052delinsGAT	XP_005248225.1:n.*3050_*3052delinsGAT
XM_006713965.2:c.*3050_*3052delinsGAT	XP_006714028.1:n.*3050_*3052delinsGAT
XM_011513846.1:c.*3050_*3052delinsGAT	XP_011512148.1:n.*3050_*3052delinsGAT
XM_011513847.1:c.*3050_*3052delinsGAT	XP_011512149.1:n.*3050_*3052delinsGAT
XM_011513848.1:c.*3050_*3052delinsGAT	XP_011512150.1:n.*3050_*3052delinsGAT
XM_011513846.2:c.*3050_*3052delinsGAT	XP_011512148.1:n.*3050_*3052delinsGAT
XM_011513847.2:c.*3050_*3052delinsGAT	XP_011512149.1:n.*3050_*3052delinsGAT
XM_017008277.1:c.*3050_*3052delinsGAT	XP_016863766.1:n.*3050_*3052delinsGAT
XM_017008278.1:c.*3050_*3052delinsGAT	XP_016863767.1:n.*3050_*3052delinsGAT
NM_016955.4:c.*3050_*3052delinsGAT MANE Select	NP_058651.3:n.*3050_*3052delinsGAT