Canonical Allele Identifier: CA1445222717

Gene: SEPSECS

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144245_25144248delinsCAGA , CM000666.2:g.25144245_25144248delinsCAGA	GRCh38
NC_000004.11:g.25145867_25145870delinsCAGA , CM000666.1:g.25145867_25145870delinsCAGA	GRCh37
NC_000004.10:g.24754965_24754968delinsCAGA	NCBI36
NG_028222.1:g.21335_21338delinsTCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.1026+526_1026+529delinsTCTG MANE Select	ENSP00000371535.2:n.1026+526_1026+529delinsTCTG
ENST00000680581.1:c.1026+526_1026+529delinsTCTG	ENSP00000506483.1:n.1026+526_1026+529delinsTCTG
ENST00000680824.1:n.2242+526_2242+529delinsTCTG
ENST00000681071.1:n.1318+526_1318+529delinsTCTG
ENST00000681341.1:n.2167+526_2167+529delinsTCTG
ENST00000681948.1:c.1281+526_1281+529delinsTCTG	ENSP00000505991.1:n.1281+526_1281+529delinsTCTG
ENST00000358971.7:c.*824+526_*824+529delinsTCTG	ENSP00000351857.3:n.*824+526_*824+529delinsTCTG
ENST00000382103.6:c.1026+526_1026+529delinsTCTG	ENSP00000371535.2:n.1026+526_1026+529delinsTCTG
ENST00000503150.1:c.308+526_308+529delinsTCTG
ENST00000505513.1:n.326+526_326+529delinsTCTG
ENST00000514585.5:c.*727+526_*727+529delinsTCTG	ENSP00000421880.1:n.*727+526_*727+529delinsTCTG
NM_016955.3:c.1026+526_1026+529delinsTCTG	NP_058651.3:n.1026+526_1026+529delinsTCTG
XM_005248168.2:c.789+526_789+529delinsTCTG	XP_005248225.1:n.789+526_789+529delinsTCTG
XM_006713965.2:c.846+526_846+529delinsTCTG	XP_006714028.1:n.846+526_846+529delinsTCTG
XM_011513846.1:c.1023+526_1023+529delinsTCTG	XP_011512148.1:n.1023+526_1023+529delinsTCTG
XM_011513847.1:c.993+526_993+529delinsTCTG	XP_011512149.1:n.993+526_993+529delinsTCTG
XM_011513848.1:c.846+526_846+529delinsTCTG	XP_011512150.1:n.846+526_846+529delinsTCTG
XM_011513846.2:c.1023+526_1023+529delinsTCTG	XP_011512148.1:n.1023+526_1023+529delinsTCTG
XM_011513847.2:c.993+526_993+529delinsTCTG	XP_011512149.1:n.993+526_993+529delinsTCTG
XM_017008277.1:c.1281+526_1281+529delinsTCTG	XP_016863766.1:n.1281+526_1281+529delinsTCTG
XM_017008278.1:c.603+526_603+529delinsTCTG	XP_016863767.1:n.603+526_603+529delinsTCTG
NM_016955.4:c.1026+526_1026+529delinsTCTG MANE Select	NP_058651.3:n.1026+526_1026+529delinsTCTG