Canonical Allele Identifier: CA2670197128

Gene: SEPSECS

Linked Data

• gnomAD v4: 4-25156339-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25156339A>C , CM000666.2:g.25156339A>C	GRCh38
NC_000004.11:g.25157961A>C , CM000666.1:g.25157961A>C	GRCh37
NC_000004.10:g.24767059A>C	NCBI36
NG_028222.1:g.9244T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.389-144T>G MANE Select	ENSP00000371535.2:n.389-144T>G
ENST00000680581.1:c.389-144T>G	ENSP00000506483.1:n.389-144T>G
ENST00000680824.1:n.1605-144T>G
ENST00000681071.1:n.681-144T>G
ENST00000681166.1:n.1436-144T>G
ENST00000681341.1:n.1530-144T>G
ENST00000681640.1:n.483-144T>G
ENST00000681948.1:c.644-144T>G	ENSP00000505991.1:n.644-144T>G
ENST00000358971.7:c.*187-144T>G	ENSP00000351857.3:n.*187-144T>G
ENST00000382103.6:c.389-144T>G	ENSP00000371535.2:n.389-144T>G
ENST00000514585.5:c.*90-144T>G	ENSP00000421880.1:n.*90-144T>G
NM_016955.3:c.389-144T>G	NP_058651.3:n.389-144T>G
XM_005248168.2:c.152-144T>G	XP_005248225.1:n.152-144T>G
XM_006713965.2:c.209-144T>G	XP_006714028.1:n.209-144T>G
XM_011513846.1:c.386-144T>G	XP_011512148.1:n.386-144T>G
XM_011513847.1:c.356-144T>G	XP_011512149.1:n.356-144T>G
XM_011513848.1:c.209-144T>G	XP_011512150.1:n.209-144T>G
XM_011513846.2:c.386-144T>G	XP_011512148.1:n.386-144T>G
XM_011513847.2:c.356-144T>G	XP_011512149.1:n.356-144T>G
XM_017008277.1:c.644-144T>G	XP_016863766.1:n.644-144T>G
XM_017008278.1:c.-35-144T>G	XP_016863767.1:n.-35-144T>G
NM_016955.4:c.389-144T>G MANE Select	NP_058651.3:n.389-144T>G