Canonical Allele Identifier: CA438732278

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25146405T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144783T>C , CM000666.2:g.25144783T>C	GRCh38
NC_000004.11:g.25146405T>C , CM000666.1:g.25146405T>C	GRCh37
NC_000004.10:g.24755503T>C	NCBI36
NG_028222.1:g.20800A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.1017A>G MANE Select	ENSP00000371535.2:p.Lys339=
ENST00000680581.1:c.1017A>G	ENSP00000506483.1:p.Lys339=
ENST00000680824.1:n.2233A>G
ENST00000681071.1:n.1309A>G
ENST00000681341.1:n.2158A>G
ENST00000681948.1:c.1272A>G	ENSP00000505991.1:p.Lys424=
ENST00000358971.7:c.*815A>G	ENSP00000351857.3:n.*815A>G
ENST00000382103.6:c.1017A>G	ENSP00000371535.2:p.Lys339=
ENST00000503150.1:c.299A>G
ENST00000505513.1:n.317A>G
ENST00000514585.5:c.*718A>G	ENSP00000421880.1:n.*718A>G
NM_016955.3:c.1017A>G	NP_058651.3:p.Lys339=
XM_005248168.2:c.780A>G	XP_005248225.1:p.Lys260=
XM_006713965.2:c.837A>G	XP_006714028.1:p.Lys279=
XM_011513846.1:c.1014A>G	XP_011512148.1:p.Lys338=
XM_011513847.1:c.984A>G	XP_011512149.1:p.Lys328=
XM_011513848.1:c.837A>G	XP_011512150.1:p.Lys279=
XM_011513846.2:c.1014A>G	XP_011512148.1:p.Lys338=
XM_011513847.2:c.984A>G	XP_011512149.1:p.Lys328=
XM_017008277.1:c.1272A>G	XP_016863766.1:p.Lys424=
XM_017008278.1:c.594A>G	XP_016863767.1:p.Lys198=
NM_016955.4:c.1017A>G MANE Select	NP_058651.3:p.Lys339=