Canonical Allele Identifier: CA2173254981

Gene: STRC

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43611237G= , CM000677.2:g.43611237G=	GRCh38
NC_000015.9:g.43903435G= , CM000677.1:g.43903435G=	GRCh37
NC_000015.8:g.41690727G=	NCBI36
NG_011636.1:g.12564C=

Transcript Alleles

HGVS	Amino-acid Change
NM_153700.2:c.3217C= MANE Select	NP_714544.1:p.Arg1073=
ENST00000450892.7:c.3217C= MANE Select	ENSP00000401513.2:p.Arg1073=
ENST00000428650.5:c.*249C=	ENSP00000415991.1:n.*249C=
ENST00000440125.5:c.*1215+262C=	ENSP00000394866.1:n.*1215+262C=
ENST00000448437.6:n.444C=
ENST00000450892.6:c.3217C=	ENSP00000401513.2:p.Arg1073=
ENST00000455136.5:c.529+262C=
ENST00000470279.1:n.531C=
ENST00000471703.5:n.356C=
ENST00000483250.5:n.528C=
ENST00000485556.5:n.587C=
ENST00000541030.5:c.1104+262C=	ENSP00000440413.1:n.1104+262C=
XM_011521277.1:c.3706C=	XP_011519579.1:p.Arg1236=
XM_011521278.1:c.3319C=	XP_011519580.1:p.Arg1107=
XM_011521279.1:c.3319C=	XP_011519581.1:p.Arg1107=