Canonical Allele Identifier: CA1445223210

Gene: SEPSECS

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144773_25144777delinsCCTTT , CM000666.2:g.25144773_25144777delinsCCTTT	GRCh38
NC_000004.11:g.25146395_25146399delinsCCTTT , CM000666.1:g.25146395_25146399delinsCCTTT	GRCh37
NC_000004.10:g.24755493_24755497delinsCCTTT	NCBI36
NG_028222.1:g.20806_20810delinsAAAGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000382103.7:c.1023_1026+1delinsAAAGG
ENST00000680581.1:c.1023_1026+1delinsAAAGG
ENST00000680824.1:n.2239_2242+1delinsAAAGG
ENST00000681071.1:n.1315_1318+1delinsAAAGG
ENST00000681341.1:n.2164_2167+1delinsAAAGG
ENST00000681948.1:c.1278_1281+1delinsAAAGG
ENST00000358971.7:c.*821_*824+1delinsAAAGG
ENST00000382103.6:c.1023_1026+1delinsAAAGG
ENST00000503150.1:c.305_308+1delinsAAAGG
ENST00000505513.1:n.323_326+1delinsAAAGG
ENST00000514585.5:c.*724_*727+1delinsAAAGG
NM_016955.3:c.1023_1026+1delinsAAAGG
XM_005248168.2:c.786_789+1delinsAAAGG
XM_006713965.2:c.843_846+1delinsAAAGG
XM_011513846.1:c.1020_1023+1delinsAAAGG
XM_011513847.1:c.990_993+1delinsAAAGG
XM_011513848.1:c.843_846+1delinsAAAGG
XM_011513846.2:c.1020_1023+1delinsAAAGG
XM_011513847.2:c.990_993+1delinsAAAGG
XM_017008277.1:c.1278_1281+1delinsAAAGG
XM_017008278.1:c.600_603+1delinsAAAGG
NM_016955.4:c.1023_1026+1delinsAAAGG