Canonical Allele Identifier: CA1060323081

Gene: SEPSECS

Linked Data

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

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144339_25144346dup , CM000666.2:g.25144339_25144346dup	GRCh38
NC_000004.11:g.25145961_25145968dup , CM000666.1:g.25145961_25145968dup	GRCh37
NC_000004.10:g.24755059_24755066dup	NCBI36
NG_028222.1:g.21249_21256dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.1026+440_1026+447dup MANE Select	ENSP00000371535.2:n.1026+440_1026+447dup
ENST00000680581.1:c.1026+440_1026+447dup	ENSP00000506483.1:n.1026+440_1026+447dup
ENST00000680824.1:n.2242+440_2242+447dup
ENST00000681071.1:n.1318+440_1318+447dup
ENST00000681341.1:n.2167+440_2167+447dup
ENST00000681948.1:c.1281+440_1281+447dup	ENSP00000505991.1:n.1281+440_1281+447dup
ENST00000358971.7:c.*824+440_*824+447dup	ENSP00000351857.3:n.*824+440_*824+447dup
ENST00000382103.6:c.1026+440_1026+447dup	ENSP00000371535.2:n.1026+440_1026+447dup
ENST00000503150.1:c.308+440_308+447dup
ENST00000505513.1:n.326+440_326+447dup
ENST00000514585.5:c.*727+440_*727+447dup	ENSP00000421880.1:n.*727+440_*727+447dup
NM_016955.3:c.1026+440_1026+447dup	NP_058651.3:n.1026+440_1026+447dup
XM_005248168.2:c.789+440_789+447dup	XP_005248225.1:n.789+440_789+447dup
XM_006713965.2:c.846+440_846+447dup	XP_006714028.1:n.846+440_846+447dup
XM_011513846.1:c.1023+440_1023+447dup	XP_011512148.1:n.1023+440_1023+447dup
XM_011513847.1:c.993+440_993+447dup	XP_011512149.1:n.993+440_993+447dup
XM_011513848.1:c.846+440_846+447dup	XP_011512150.1:n.846+440_846+447dup
XM_011513846.2:c.1023+440_1023+447dup	XP_011512148.1:n.1023+440_1023+447dup
XM_011513847.2:c.993+440_993+447dup	XP_011512149.1:n.993+440_993+447dup
XM_017008277.1:c.1281+440_1281+447dup	XP_016863766.1:n.1281+440_1281+447dup
XM_017008278.1:c.603+440_603+447dup	XP_016863767.1:n.603+440_603+447dup
NM_016955.4:c.1026+440_1026+447dup MANE Select	NP_058651.3:n.1026+440_1026+447dup