Canonical Allele Identifier: CA2173254579

Gene: STRC

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43610326A= , CM000677.2:g.43610326A=	GRCh38
NC_000015.9:g.43902524A= , CM000677.1:g.43902524A=	GRCh37
NC_000015.8:g.41689816A=	NCBI36
NG_011636.1:g.13475T=

Transcript Alleles

HGVS	Amino-acid Change
NM_153700.2:c.3484T= MANE Select	NP_714544.1:p.Trp1162=
ENST00000450892.7:c.3484T= MANE Select	ENSP00000401513.2:p.Trp1162=
ENST00000428650.5:c.*516T=	ENSP00000415991.1:n.*516T=
ENST00000440125.5:c.*1276T=	ENSP00000394866.1:n.*1276T=
ENST00000448437.6:n.1355T=
ENST00000450892.6:c.3484T=	ENSP00000401513.2:p.Trp1162=
ENST00000455136.5:c.530-992T=
ENST00000471703.5:n.1267T=
ENST00000485556.5:n.1498T=
ENST00000541030.5:c.1165T=	ENSP00000440413.1:p.Trp389=
XM_011521277.1:c.3973T=	XP_011519579.1:p.Trp1325=
XM_011521278.1:c.3589T=	XP_011519580.1:p.Trp1197=
XM_011521279.1:c.3589T=	XP_011519581.1:p.Trp1197=