Canonical Allele Identifier: CA2173254575

Gene: STRC

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43610317G= , CM000677.2:g.43610317G=	GRCh38
NC_000015.9:g.43902515G= , CM000677.1:g.43902515G=	GRCh37
NC_000015.8:g.41689807G=	NCBI36
NG_011636.1:g.13484C=

Transcript Alleles

HGVS	Amino-acid Change
NM_153700.2:c.3493C= MANE Select	NP_714544.1:p.Gln1165=
ENST00000450892.7:c.3493C= MANE Select	ENSP00000401513.2:p.Gln1165=
ENST00000428650.5:c.*525C=	ENSP00000415991.1:n.*525C=
ENST00000440125.5:c.*1285C=	ENSP00000394866.1:n.*1285C=
ENST00000448437.6:n.1364C=
ENST00000450892.6:c.3493C=	ENSP00000401513.2:p.Gln1165=
ENST00000455136.5:c.530-983C=
ENST00000471703.5:n.1276C=
ENST00000485556.5:n.1507C=
ENST00000541030.5:c.1174C=	ENSP00000440413.1:p.Gln392=
XM_011521277.1:c.3982C=	XP_011519579.1:p.Gln1328=
XM_011521278.1:c.3598C=	XP_011519580.1:p.Gln1200=
XM_011521279.1:c.3598C=	XP_011519581.1:p.Gln1200=