Canonical Allele Identifier: CA2173250683

Gene: STRC CKMT1B

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43603385G= , CM000677.2:g.43603385G=	GRCh38
NC_000015.9:g.43895583G= , CM000677.1:g.43895583G=	GRCh37
NC_000015.8:g.41682875G=	NCBI36
NG_011636.1:g.20416C=

Transcript Alleles

HGVS	Amino-acid Change
NM_153700.2:c.4402C= (STRC) MANE Select	NP_714544.1:p.Arg1468=
ENST00000450892.7:c.4402C= (STRC) MANE Select	ENSP00000401513.2:p.Arg1468=
ENST00000411560.1:n.143-1399G= (CKMT1B)
ENST00000428650.5:c.*1578+611C= (STRC)	ENSP00000415991.1:n.*1578+611C=
ENST00000440125.5:c.*2194C= (STRC)	ENSP00000394866.1:n.*2194C=
ENST00000448437.6:n.1666-1834C= (STRC)
ENST00000450892.6:c.4402C= (STRC)	ENSP00000401513.2:p.Arg1468=
ENST00000471703.5:n.2356C= (STRC)
ENST00000485556.5:n.3257C= (STRC)
ENST00000493750.1:n.198C= (STRC)
ENST00000541030.5:c.2083C= (STRC)	ENSP00000440413.1:p.Arg695=
XM_011521277.1:c.4891C= (STRC)	XP_011519579.1:p.Arg1631=
XM_011521278.1:c.4507C= (STRC)	XP_011519580.1:p.Arg1503=
XM_011521279.1:c.4507C= (STRC)	XP_011519581.1:p.Arg1503=