Canonical Allele Identifier: CA356536850

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25146450A>C (hg19) ; chr4:g.25144828A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144828A>C , CM000666.2:g.25144828A>C	GRCh38
NC_000004.11:g.25146450A>C , CM000666.1:g.25146450A>C	GRCh37
NC_000004.10:g.24755548A>C	NCBI36
NG_028222.1:g.20755T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.972T>G MANE Select	ENSP00000371535.2:p.Ile324Met
ENST00000680581.1:c.972T>G	ENSP00000506483.1:p.Ile324Met
ENST00000680824.1:n.2188T>G
ENST00000681071.1:n.1264T>G
ENST00000681341.1:n.2113T>G
ENST00000681948.1:c.1227T>G	ENSP00000505991.1:p.Ile409Met
ENST00000358971.7:c.*770T>G	ENSP00000351857.3:n.*770T>G
ENST00000382103.6:c.972T>G	ENSP00000371535.2:p.Ile324Met
ENST00000503150.1:c.254T>G
ENST00000505513.1:n.272T>G
ENST00000514585.5:c.*673T>G	ENSP00000421880.1:n.*673T>G
NM_016955.3:c.972T>G	NP_058651.3:p.Ile324Met
XM_005248168.2:c.735T>G	XP_005248225.1:p.Ile245Met
XM_006713965.2:c.792T>G	XP_006714028.1:p.Ile264Met
XM_011513846.1:c.969T>G	XP_011512148.1:p.Ile323Met
XM_011513847.1:c.939T>G	XP_011512149.1:p.Ile313Met
XM_011513848.1:c.792T>G	XP_011512150.1:p.Ile264Met
XM_011513846.2:c.969T>G	XP_011512148.1:p.Ile323Met
XM_011513847.2:c.939T>G	XP_011512149.1:p.Ile313Met
XM_017008277.1:c.1227T>G	XP_016863766.1:p.Ile409Met
XM_017008278.1:c.549T>G	XP_016863767.1:p.Ile183Met
NM_016955.4:c.972T>G MANE Select	NP_058651.3:p.Ile324Met