Canonical Allele Identifier: CA438732288

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25146420A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144798A>G , CM000666.2:g.25144798A>G	GRCh38
NC_000004.11:g.25146420A>G , CM000666.1:g.25146420A>G	GRCh37
NC_000004.10:g.24755518A>G	NCBI36
NG_028222.1:g.20785T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.1002T>C MANE Select	ENSP00000371535.2:p.Tyr334=
ENST00000680581.1:c.1002T>C	ENSP00000506483.1:p.Tyr334=
ENST00000680824.1:n.2218T>C
ENST00000681071.1:n.1294T>C
ENST00000681341.1:n.2143T>C
ENST00000681948.1:c.1257T>C	ENSP00000505991.1:p.Tyr419=
ENST00000358971.7:c.*800T>C	ENSP00000351857.3:n.*800T>C
ENST00000382103.6:c.1002T>C	ENSP00000371535.2:p.Tyr334=
ENST00000503150.1:c.284T>C
ENST00000505513.1:n.302T>C
ENST00000514585.5:c.*703T>C	ENSP00000421880.1:n.*703T>C
NM_016955.3:c.1002T>C	NP_058651.3:p.Tyr334=
XM_005248168.2:c.765T>C	XP_005248225.1:p.Tyr255=
XM_006713965.2:c.822T>C	XP_006714028.1:p.Tyr274=
XM_011513846.1:c.999T>C	XP_011512148.1:p.Tyr333=
XM_011513847.1:c.969T>C	XP_011512149.1:p.Tyr323=
XM_011513848.1:c.822T>C	XP_011512150.1:p.Tyr274=
XM_011513846.2:c.999T>C	XP_011512148.1:p.Tyr333=
XM_011513847.2:c.969T>C	XP_011512149.1:p.Tyr323=
XM_017008277.1:c.1257T>C	XP_016863766.1:p.Tyr419=
XM_017008278.1:c.579T>C	XP_016863767.1:p.Tyr193=
NM_016955.4:c.1002T>C MANE Select	NP_058651.3:p.Tyr334=