Canonical Allele Identifier: CA2670220934

Gene: SEPSECS

Linked Data

• gnomAD v4: 4-25120544-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25120544G>T , CM000666.2:g.25120544G>T	GRCh38
NC_000004.11:g.25122166G>T , CM000666.1:g.25122166G>T	GRCh37
NC_000004.10:g.24731264G>T	NCBI36
NG_028222.1:g.45039C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.*3387C>A MANE Select	ENSP00000371535.2:n.*3387C>A
ENST00000680581.1:c.*3767C>A	ENSP00000506483.1:n.*3767C>A
ENST00000680824.1:n.6109C>A
ENST00000681071.1:n.5185C>A
ENST00000681341.1:n.5940C>A
ENST00000681374.1:n.4249C>A
ENST00000681948.1:c.*3387C>A	ENSP00000505991.1:n.*3387C>A
ENST00000382103.6:c.*3387C>A	ENSP00000371535.2:n.*3387C>A
NM_016955.3:c.*3387C>A	NP_058651.3:n.*3387C>A
XM_005248168.2:c.*3387C>A	XP_005248225.1:n.*3387C>A
XM_006713965.2:c.*3387C>A	XP_006714028.1:n.*3387C>A
XM_011513846.1:c.*3387C>A	XP_011512148.1:n.*3387C>A
XM_011513847.1:c.*3387C>A	XP_011512149.1:n.*3387C>A
XM_011513848.1:c.*3387C>A	XP_011512150.1:n.*3387C>A
XM_011513846.2:c.*3387C>A	XP_011512148.1:n.*3387C>A
XM_011513847.2:c.*3387C>A	XP_011512149.1:n.*3387C>A
XM_017008277.1:c.*3387C>A	XP_016863766.1:n.*3387C>A
XM_017008278.1:c.*3387C>A	XP_016863767.1:n.*3387C>A
NM_016955.4:c.*3387C>A MANE Select	NP_058651.3:n.*3387C>A