Canonical Allele Identifier: CA1445223264

Gene: SEPSECS

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144847G= , CM000666.2:g.25144847G=	GRCh38
NC_000004.11:g.25146469G= , CM000666.1:g.25146469G=	GRCh37
NC_000004.10:g.24755567G=	NCBI36
NG_028222.1:g.20736C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382103.7:c.953C= MANE Select	ENSP00000371535.2:p.Pro318=
ENST00000680581.1:c.953C=	ENSP00000506483.1:p.Pro318=
ENST00000680824.1:n.2169C=
ENST00000681071.1:n.1245C=
ENST00000681341.1:n.2094C=
ENST00000681948.1:c.1208C=	ENSP00000505991.1:p.Pro403=
ENST00000358971.7:c.*751C=	ENSP00000351857.3:n.*751C=
ENST00000382103.6:c.953C=	ENSP00000371535.2:p.Pro318=
ENST00000503150.1:c.235C=
ENST00000505513.1:n.253C=
ENST00000514585.5:c.*654C=	ENSP00000421880.1:n.*654C=
NM_016955.3:c.953C=	NP_058651.3:p.Pro318=
XM_005248168.2:c.716C=	XP_005248225.1:p.Pro239=
XM_006713965.2:c.773C=	XP_006714028.1:p.Pro258=
XM_011513846.1:c.950C=	XP_011512148.1:p.Pro317=
XM_011513847.1:c.920C=	XP_011512149.1:p.Pro307=
XM_011513848.1:c.773C=	XP_011512150.1:p.Pro258=
XM_011513846.2:c.950C=	XP_011512148.1:p.Pro317=
XM_011513847.2:c.920C=	XP_011512149.1:p.Pro307=
XM_017008277.1:c.1208C=	XP_016863766.1:p.Pro403=
XM_017008278.1:c.530C=	XP_016863767.1:p.Pro177=
NM_016955.4:c.953C= MANE Select	NP_058651.3:p.Pro318=