Canonical Allele Identifier: CA2670221017

Gene: SEPSECS

Linked Data

• gnomAD v4: 4-25120834-ACTACTAATT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25120836_25120844del , CM000666.2:g.25120836_25120844del	GRCh38
NC_000004.11:g.25122458_25122466del , CM000666.1:g.25122458_25122466del	GRCh37
NC_000004.10:g.24731556_24731564del	NCBI36
NG_028222.1:g.44740_44748del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.*3088_*3096del MANE Select	ENSP00000371535.2:n.*3088_*3096del
ENST00000680581.1:c.*3468_*3476del	ENSP00000506483.1:n.*3468_*3476del
ENST00000680824.1:n.5810_5818del
ENST00000681071.1:n.4886_4894del
ENST00000681341.1:n.5641_5649del
ENST00000681374.1:n.3950_3958del
ENST00000681948.1:c.*3088_*3096del	ENSP00000505991.1:n.*3088_*3096del
ENST00000382103.6:c.*3088_*3096del	ENSP00000371535.2:n.*3088_*3096del
NM_016955.3:c.*3088_*3096del	NP_058651.3:n.*3088_*3096del
XM_005248168.2:c.*3088_*3096del	XP_005248225.1:n.*3088_*3096del
XM_006713965.2:c.*3088_*3096del	XP_006714028.1:n.*3088_*3096del
XM_011513846.1:c.*3088_*3096del	XP_011512148.1:n.*3088_*3096del
XM_011513847.1:c.*3088_*3096del	XP_011512149.1:n.*3088_*3096del
XM_011513848.1:c.*3088_*3096del	XP_011512150.1:n.*3088_*3096del
XM_011513846.2:c.*3088_*3096del	XP_011512148.1:n.*3088_*3096del
XM_011513847.2:c.*3088_*3096del	XP_011512149.1:n.*3088_*3096del
XM_017008277.1:c.*3088_*3096del	XP_016863766.1:n.*3088_*3096del
XM_017008278.1:c.*3088_*3096del	XP_016863767.1:n.*3088_*3096del
NM_016955.4:c.*3088_*3096del MANE Select	NP_058651.3:n.*3088_*3096del