Canonical Allele Identifier: CA1060323065

Gene: SEPSECS

Linked Data

• gnomAD v3: 4-25144326-C-CAAAAAAAAAAAAAAAAAAAAA
• gnomAD v4: 4-25144326-C-CAAAAAAAAAAAAAAAAAAAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144346_25144347insAAAAAAAAAAAAAAAAAAAAA , CM000666.2:g.25144346_25144347insAAAAAAAAAAAAAAAAAAAAA	GRCh38
NC_000004.11:g.25145968_25145969insAAAAAAAAAAAAAAAAAAAAA , CM000666.1:g.25145968_25145969insAAAAAAAAAAAAAAAAAAAAA	GRCh37
NC_000004.10:g.24755066_24755067insAAAAAAAAAAAAAAAAAAAAA	NCBI36
NG_028222.1:g.21256_21257insTTTTTTTTTTTTTTTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.1026+447_1026+448insTTTTTTTTTTTTTTTTTTTTT MANE Select	ENSP00000371535.2:n.1026+447_1026+448insTTTTTTTTTTTTTTTTTTTTT...
ENST00000680581.1:c.1026+447_1026+448insTTTTTTTTTTTTTTTTTTTTT	ENSP00000506483.1:n.1026+447_1026+448insTTTTTTTTTTTTTTTTTTTTT...
ENST00000680824.1:n.2242+447_2242+448insTTTTTTTTTTTTTTTTTTTTT
ENST00000681071.1:n.1318+447_1318+448insTTTTTTTTTTTTTTTTTTTTT
ENST00000681341.1:n.2167+447_2167+448insTTTTTTTTTTTTTTTTTTTTT
ENST00000681948.1:c.1281+447_1281+448insTTTTTTTTTTTTTTTTTTTTT	ENSP00000505991.1:n.1281+447_1281+448insTTTTTTTTTTTTTTTTTTTTT...
ENST00000358971.7:c.*824+447_*824+448insTTTTTTTTTTTTTTTTTTTTT	ENSP00000351857.3:n.*824+447_*824+448insTTTTTTTTTTTTTTTTTTTTT...
ENST00000382103.6:c.1026+447_1026+448insTTTTTTTTTTTTTTTTTTTTT	ENSP00000371535.2:n.1026+447_1026+448insTTTTTTTTTTTTTTTTTTTTT...
ENST00000503150.1:c.308+447_308+448insTTTTTTTTTTTTTTTTTTTTT
ENST00000505513.1:n.326+447_326+448insTTTTTTTTTTTTTTTTTTTTT
ENST00000514585.5:c.*727+447_*727+448insTTTTTTTTTTTTTTTTTTTTT	ENSP00000421880.1:n.*727+447_*727+448insTTTTTTTTTTTTTTTTTTTTT...
NM_016955.3:c.1026+447_1026+448insTTTTTTTTTTTTTTTTTTTTT	NP_058651.3:n.1026+447_1026+448insTTTTTTTTTTTTTTTTTTTTT
XM_005248168.2:c.789+447_789+448insTTTTTTTTTTTTTTTTTTTTT	XP_005248225.1:n.789+447_789+448insTTTTTTTTTTTTTTTTTTTTT
XM_006713965.2:c.846+447_846+448insTTTTTTTTTTTTTTTTTTTTT	XP_006714028.1:n.846+447_846+448insTTTTTTTTTTTTTTTTTTTTT
XM_011513846.1:c.1023+447_1023+448insTTTTTTTTTTTTTTTTTTTTT	XP_011512148.1:n.1023+447_1023+448insTTTTTTTTTTTTTTTTTTTTT
XM_011513847.1:c.993+447_993+448insTTTTTTTTTTTTTTTTTTTTT	XP_011512149.1:n.993+447_993+448insTTTTTTTTTTTTTTTTTTTTT
XM_011513848.1:c.846+447_846+448insTTTTTTTTTTTTTTTTTTTTT	XP_011512150.1:n.846+447_846+448insTTTTTTTTTTTTTTTTTTTTT
XM_011513846.2:c.1023+447_1023+448insTTTTTTTTTTTTTTTTTTTTT	XP_011512148.1:n.1023+447_1023+448insTTTTTTTTTTTTTTTTTTTTT
XM_011513847.2:c.993+447_993+448insTTTTTTTTTTTTTTTTTTTTT	XP_011512149.1:n.993+447_993+448insTTTTTTTTTTTTTTTTTTTTT
XM_017008277.1:c.1281+447_1281+448insTTTTTTTTTTTTTTTTTTTTT	XP_016863766.1:n.1281+447_1281+448insTTTTTTTTTTTTTTTTTTTTT
XM_017008278.1:c.603+447_603+448insTTTTTTTTTTTTTTTTTTTTT	XP_016863767.1:n.603+447_603+448insTTTTTTTTTTTTTTTTTTTTT
NM_016955.4:c.1026+447_1026+448insTTTTTTTTTTTTTTTTTTTTT MANE Select	NP_058651.3:n.1026+447_1026+448insTTTTTTTTTTTTTTTTTTTTT