Canonical Allele Identifier: CA356536695

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25146413G>C (hg19) ; chr4:g.25144791G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144791G>C , CM000666.2:g.25144791G>C	GRCh38
NC_000004.11:g.25146413G>C , CM000666.1:g.25146413G>C	GRCh37
NC_000004.10:g.24755511G>C	NCBI36
NG_028222.1:g.20792C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.1009C>G MANE Select	ENSP00000371535.2:p.Leu337Val
ENST00000680581.1:c.1009C>G	ENSP00000506483.1:p.Leu337Val
ENST00000680824.1:n.2225C>G
ENST00000681071.1:n.1301C>G
ENST00000681341.1:n.2150C>G
ENST00000681948.1:c.1264C>G	ENSP00000505991.1:p.Leu422Val
ENST00000358971.7:c.*807C>G	ENSP00000351857.3:n.*807C>G
ENST00000382103.6:c.1009C>G	ENSP00000371535.2:p.Leu337Val
ENST00000503150.1:c.291C>G
ENST00000505513.1:n.309C>G
ENST00000514585.5:c.*710C>G	ENSP00000421880.1:n.*710C>G
NM_016955.3:c.1009C>G	NP_058651.3:p.Leu337Val
XM_005248168.2:c.772C>G	XP_005248225.1:p.Leu258Val
XM_006713965.2:c.829C>G	XP_006714028.1:p.Leu277Val
XM_011513846.1:c.1006C>G	XP_011512148.1:p.Leu336Val
XM_011513847.1:c.976C>G	XP_011512149.1:p.Leu326Val
XM_011513848.1:c.829C>G	XP_011512150.1:p.Leu277Val
XM_011513846.2:c.1006C>G	XP_011512148.1:p.Leu336Val
XM_011513847.2:c.976C>G	XP_011512149.1:p.Leu326Val
XM_017008277.1:c.1264C>G	XP_016863766.1:p.Leu422Val
XM_017008278.1:c.586C>G	XP_016863767.1:p.Leu196Val
NM_016955.4:c.1009C>G MANE Select	NP_058651.3:p.Leu337Val