Canonical Allele Identifier: CA2607850080

Gene: SEPSECS

Linked Data

• gnomAD v4: 4-25144352-AGCT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144353_25144355del , CM000666.2:g.25144353_25144355del	GRCh38
NC_000004.11:g.25145975_25145977del , CM000666.1:g.25145975_25145977del	GRCh37
NC_000004.10:g.24755073_24755075del	NCBI36
NG_028222.1:g.21228_21230del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.1026+419_1026+421del MANE Select	ENSP00000371535.2:n.1026+419_1026+421del
ENST00000680581.1:c.1026+419_1026+421del	ENSP00000506483.1:n.1026+419_1026+421del
ENST00000680824.1:n.2242+419_2242+421del
ENST00000681071.1:n.1318+419_1318+421del
ENST00000681341.1:n.2167+419_2167+421del
ENST00000681948.1:c.1281+419_1281+421del	ENSP00000505991.1:n.1281+419_1281+421del
ENST00000358971.7:c.*824+419_*824+421del	ENSP00000351857.3:n.*824+419_*824+421del
ENST00000382103.6:c.1026+419_1026+421del	ENSP00000371535.2:n.1026+419_1026+421del
ENST00000503150.1:c.308+419_308+421del
ENST00000505513.1:n.326+419_326+421del
ENST00000514585.5:c.*727+419_*727+421del	ENSP00000421880.1:n.*727+419_*727+421del
NM_016955.3:c.1026+419_1026+421del	NP_058651.3:n.1026+419_1026+421del
XM_005248168.2:c.789+419_789+421del	XP_005248225.1:n.789+419_789+421del
XM_006713965.2:c.846+419_846+421del	XP_006714028.1:n.846+419_846+421del
XM_011513846.1:c.1023+419_1023+421del	XP_011512148.1:n.1023+419_1023+421del
XM_011513847.1:c.993+419_993+421del	XP_011512149.1:n.993+419_993+421del
XM_011513848.1:c.846+419_846+421del	XP_011512150.1:n.846+419_846+421del
XM_011513846.2:c.1023+419_1023+421del	XP_011512148.1:n.1023+419_1023+421del
XM_011513847.2:c.993+419_993+421del	XP_011512149.1:n.993+419_993+421del
XM_017008277.1:c.1281+419_1281+421del	XP_016863766.1:n.1281+419_1281+421del
XM_017008278.1:c.603+419_603+421del	XP_016863767.1:n.603+419_603+421del
NM_016955.4:c.1026+419_1026+421del MANE Select	NP_058651.3:n.1026+419_1026+421del