Canonical Allele Identifier: CA2670196460

Gene: SEPSECS

Linked Data

• gnomAD v4: 4-25144673-G-GTGCTCCAAATCATTGGTGTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144674_25144675insGCTCCAAATCATTGGTGTTTT , CM000666.2:g.25144674_25144675insGCTCCAAATCATTGGTGTTTT	GRCh38
NC_000004.11:g.25146296_25146297insGCTCCAAATCATTGGTGTTTT , CM000666.1:g.25146296_25146297insGCTCCAAATCATTGGTGTTTT	GRCh37
NC_000004.10:g.24755394_24755395insGCTCCAAATCATTGGTGTTTT	NCBI36
NG_028222.1:g.20909_20910insAAACACCAATGATTTGGAGCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.1026+100_1026+101insAAACACCAATGATTTGGAGCA MANE Select	ENSP00000371535.2:n.1026+100_1026+101insAAACACCAATGATTTGGAGCA...
ENST00000680581.1:c.1026+100_1026+101insAAACACCAATGATTTGGAGCA	ENSP00000506483.1:n.1026+100_1026+101insAAACACCAATGATTTGGAGCA...
ENST00000680824.1:n.2242+100_2242+101insAAACACCAATGATTTGGAGCA
ENST00000681071.1:n.1318+100_1318+101insAAACACCAATGATTTGGAGCA
ENST00000681341.1:n.2167+100_2167+101insAAACACCAATGATTTGGAGCA
ENST00000681948.1:c.1281+100_1281+101insAAACACCAATGATTTGGAGCA	ENSP00000505991.1:n.1281+100_1281+101insAAACACCAATGATTTGGAGCA...
ENST00000358971.7:c.*824+100_*824+101insAAACACCAATGATTTGGAGCA	ENSP00000351857.3:n.*824+100_*824+101insAAACACCAATGATTTGGAGCA...
ENST00000382103.6:c.1026+100_1026+101insAAACACCAATGATTTGGAGCA	ENSP00000371535.2:n.1026+100_1026+101insAAACACCAATGATTTGGAGCA...
ENST00000503150.1:c.308+100_308+101insAAACACCAATGATTTGGAGCA
ENST00000505513.1:n.326+100_326+101insAAACACCAATGATTTGGAGCA
ENST00000514585.5:c.*727+100_*727+101insAAACACCAATGATTTGGAGCA	ENSP00000421880.1:n.*727+100_*727+101insAAACACCAATGATTTGGAGCA...
NM_016955.3:c.1026+100_1026+101insAAACACCAATGATTTGGAGCA	NP_058651.3:n.1026+100_1026+101insAAACACCAATGATTTGGAGCA
XM_005248168.2:c.789+100_789+101insAAACACCAATGATTTGGAGCA	XP_005248225.1:n.789+100_789+101insAAACACCAATGATTTGGAGCA
XM_006713965.2:c.846+100_846+101insAAACACCAATGATTTGGAGCA	XP_006714028.1:n.846+100_846+101insAAACACCAATGATTTGGAGCA
XM_011513846.1:c.1023+100_1023+101insAAACACCAATGATTTGGAGCA	XP_011512148.1:n.1023+100_1023+101insAAACACCAATGATTTGGAGCA
XM_011513847.1:c.993+100_993+101insAAACACCAATGATTTGGAGCA	XP_011512149.1:n.993+100_993+101insAAACACCAATGATTTGGAGCA
XM_011513848.1:c.846+100_846+101insAAACACCAATGATTTGGAGCA	XP_011512150.1:n.846+100_846+101insAAACACCAATGATTTGGAGCA
XM_011513846.2:c.1023+100_1023+101insAAACACCAATGATTTGGAGCA	XP_011512148.1:n.1023+100_1023+101insAAACACCAATGATTTGGAGCA
XM_011513847.2:c.993+100_993+101insAAACACCAATGATTTGGAGCA	XP_011512149.1:n.993+100_993+101insAAACACCAATGATTTGGAGCA
XM_017008277.1:c.1281+100_1281+101insAAACACCAATGATTTGGAGCA	XP_016863766.1:n.1281+100_1281+101insAAACACCAATGATTTGGAGCA
XM_017008278.1:c.603+100_603+101insAAACACCAATGATTTGGAGCA	XP_016863767.1:n.603+100_603+101insAAACACCAATGATTTGGAGCA
NM_016955.4:c.1026+100_1026+101insAAACACCAATGATTTGGAGCA MANE Select	NP_058651.3:n.1026+100_1026+101insAAACACCAATGATTTGGAGCA