Canonical Allele Identifier: CA1445222802

Gene: SEPSECS

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144326_25144338delinsCAAAAAAAAAAAA , CM000666.2:g.25144326_25144338delinsCAAAAAAAAAAAA	GRCh38
NC_000004.11:g.25145948_25145960delinsCAAAAAAAAAAAA , CM000666.1:g.25145948_25145960delinsCAAAAAAAAAAAA	GRCh37
NC_000004.10:g.24755046_24755058delinsCAAAAAAAAAAAA	NCBI36
NG_028222.1:g.21245_21257delinsTTTTTTTTTTTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.1026+436_1026+448delinsTTTTTTTTTTTTG MANE Select	ENSP00000371535.2:n.1026+436_1026+448delinsTTTTTTTTTTTTG
ENST00000680581.1:c.1026+436_1026+448delinsTTTTTTTTTTTTG	ENSP00000506483.1:n.1026+436_1026+448delinsTTTTTTTTTTTTG
ENST00000680824.1:n.2242+436_2242+448delinsTTTTTTTTTTTTG
ENST00000681071.1:n.1318+436_1318+448delinsTTTTTTTTTTTTG
ENST00000681341.1:n.2167+436_2167+448delinsTTTTTTTTTTTTG
ENST00000681948.1:c.1281+436_1281+448delinsTTTTTTTTTTTTG	ENSP00000505991.1:n.1281+436_1281+448delinsTTTTTTTTTTTTG
ENST00000358971.7:c.*824+436_*824+448delinsTTTTTTTTTTTTG	ENSP00000351857.3:n.*824+436_*824+448delinsTTTTTTTTTTTTG
ENST00000382103.6:c.1026+436_1026+448delinsTTTTTTTTTTTTG	ENSP00000371535.2:n.1026+436_1026+448delinsTTTTTTTTTTTTG
ENST00000503150.1:c.308+436_308+448delinsTTTTTTTTTTTTG
ENST00000505513.1:n.326+436_326+448delinsTTTTTTTTTTTTG
ENST00000514585.5:c.*727+436_*727+448delinsTTTTTTTTTTTTG	ENSP00000421880.1:n.*727+436_*727+448delinsTTTTTTTTTTTTG
NM_016955.3:c.1026+436_1026+448delinsTTTTTTTTTTTTG	NP_058651.3:n.1026+436_1026+448delinsTTTTTTTTTTTTG
XM_005248168.2:c.789+436_789+448delinsTTTTTTTTTTTTG	XP_005248225.1:n.789+436_789+448delinsTTTTTTTTTTTTG
XM_006713965.2:c.846+436_846+448delinsTTTTTTTTTTTTG	XP_006714028.1:n.846+436_846+448delinsTTTTTTTTTTTTG
XM_011513846.1:c.1023+436_1023+448delinsTTTTTTTTTTTTG	XP_011512148.1:n.1023+436_1023+448delinsTTTTTTTTTTTTG
XM_011513847.1:c.993+436_993+448delinsTTTTTTTTTTTTG	XP_011512149.1:n.993+436_993+448delinsTTTTTTTTTTTTG
XM_011513848.1:c.846+436_846+448delinsTTTTTTTTTTTTG	XP_011512150.1:n.846+436_846+448delinsTTTTTTTTTTTTG
XM_011513846.2:c.1023+436_1023+448delinsTTTTTTTTTTTTG	XP_011512148.1:n.1023+436_1023+448delinsTTTTTTTTTTTTG
XM_011513847.2:c.993+436_993+448delinsTTTTTTTTTTTTG	XP_011512149.1:n.993+436_993+448delinsTTTTTTTTTTTTG
XM_017008277.1:c.1281+436_1281+448delinsTTTTTTTTTTTTG	XP_016863766.1:n.1281+436_1281+448delinsTTTTTTTTTTTTG
XM_017008278.1:c.603+436_603+448delinsTTTTTTTTTTTTG	XP_016863767.1:n.603+436_603+448delinsTTTTTTTTTTTTG
NM_016955.4:c.1026+436_1026+448delinsTTTTTTTTTTTTG MANE Select	NP_058651.3:n.1026+436_1026+448delinsTTTTTTTTTTTTG