Canonical Allele Identifier: CA3212272762

Gene: STRC

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43611298G= , CM000677.2:g.43611298G=	GRCh38
NC_000015.9:g.43903496G= , CM000677.1:g.43903496G=	GRCh37
NC_000015.8:g.41690788G=	NCBI36
NG_011636.1:g.12503C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.3156C= MANE Select	ENSP00000401513.2:p.Leu1052=
ENST00000428650.5:c.*188C=	ENSP00000415991.1:n.*188C=
ENST00000440125.5:c.*1215+201C=	ENSP00000394866.1:n.*1215+201C=
ENST00000448437.6:n.383C=
ENST00000450892.6:c.3156C=	ENSP00000401513.2:p.Leu1052=
ENST00000455136.5:c.529+201C=
ENST00000470279.1:n.470C=
ENST00000471703.5:n.295C=
ENST00000483250.5:n.467C=
ENST00000485556.5:n.526C=
ENST00000541030.5:c.1104+201C=	ENSP00000440413.1:n.1104+201C=
NM_153700.2:c.3156C= MANE Select	NP_714544.1:p.Leu1052=
XM_011521277.1:c.3645C=	XP_011519579.1:p.Leu1215=
XM_011521278.1:c.3258C=	XP_011519580.1:p.Leu1086=
XM_011521279.1:c.3258C=	XP_011519581.1:p.Leu1086=