Canonical Allele Identifier: CA356536945

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25146473A>G (hg19) ; chr4:g.25144851A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144851A>G , CM000666.2:g.25144851A>G	GRCh38
NC_000004.11:g.25146473A>G , CM000666.1:g.25146473A>G	GRCh37
NC_000004.10:g.24755571A>G	NCBI36
NG_028222.1:g.20732T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.949T>C MANE Select	ENSP00000371535.2:p.Ser317Pro
ENST00000680581.1:c.949T>C	ENSP00000506483.1:p.Ser317Pro
ENST00000680824.1:n.2165T>C
ENST00000681071.1:n.1241T>C
ENST00000681341.1:n.2090T>C
ENST00000681948.1:c.1204T>C	ENSP00000505991.1:p.Ser402Pro
ENST00000358971.7:c.*747T>C	ENSP00000351857.3:n.*747T>C
ENST00000382103.6:c.949T>C	ENSP00000371535.2:p.Ser317Pro
ENST00000503150.1:c.231T>C
ENST00000505513.1:n.249T>C
ENST00000514585.5:c.*650T>C	ENSP00000421880.1:n.*650T>C
NM_016955.3:c.949T>C	NP_058651.3:p.Ser317Pro
XM_005248168.2:c.712T>C	XP_005248225.1:p.Ser238Pro
XM_006713965.2:c.769T>C	XP_006714028.1:p.Ser257Pro
XM_011513846.1:c.946T>C	XP_011512148.1:p.Ser316Pro
XM_011513847.1:c.916T>C	XP_011512149.1:p.Ser306Pro
XM_011513848.1:c.769T>C	XP_011512150.1:p.Ser257Pro
XM_011513846.2:c.946T>C	XP_011512148.1:p.Ser316Pro
XM_011513847.2:c.916T>C	XP_011512149.1:p.Ser306Pro
XM_017008277.1:c.1204T>C	XP_016863766.1:p.Ser402Pro
XM_017008278.1:c.526T>C	XP_016863767.1:p.Ser176Pro
NM_016955.4:c.949T>C MANE Select	NP_058651.3:p.Ser317Pro