Canonical Allele Identifier: CA2173253724

Gene: STRC

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43608091G= , CM000677.2:g.43608091G=	GRCh38
NC_000015.9:g.43900289G= , CM000677.1:g.43900289G=	GRCh37
NC_000015.8:g.41687581G=	NCBI36
NG_011636.1:g.15710C=

Transcript Alleles

HGVS	Amino-acid Change
NM_153700.2:c.3670C= MANE Select	NP_714544.1:p.Arg1224=
ENST00000450892.7:c.3670C= MANE Select	ENSP00000401513.2:p.Arg1224=
ENST00000428650.5:c.*702C=	ENSP00000415991.1:n.*702C=
ENST00000440125.5:c.*1462C=	ENSP00000394866.1:n.*1462C=
ENST00000448437.6:n.1541C=
ENST00000450892.6:c.3670C=	ENSP00000401513.2:p.Arg1224=
ENST00000455136.5:c.701C=
ENST00000471703.5:n.1453C=
ENST00000485556.5:n.2661C=
ENST00000541030.5:c.1351C=	ENSP00000440413.1:p.Arg451=
XM_011521277.1:c.4159C=	XP_011519579.1:p.Arg1387=
XM_011521278.1:c.3775C=	XP_011519580.1:p.Arg1259=
XM_011521279.1:c.3775C=	XP_011519581.1:p.Arg1259=