Canonical Allele Identifier: CA2173248588

Gene: STRC CKMT1B

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43601527G= , CM000677.2:g.43601527G=	GRCh38
NC_000015.9:g.43893725G= , CM000677.1:g.43893725G=	GRCh37
NC_000015.8:g.41681017G=	NCBI36
NG_011636.1:g.22274C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.4570C= (STRC) MANE Select	ENSP00000401513.2:p.Arg1524=
ENST00000411560.1:n.142+1994G= (CKMT1B)
ENST00000428650.5:c.*1603C= (STRC)	ENSP00000415991.1:n.*1603C=
ENST00000440125.5:c.*2362C= (STRC)	ENSP00000394866.1:n.*2362C=
ENST00000448437.6:n.1690C= (STRC)
ENST00000450892.6:c.4570C= (STRC)	ENSP00000401513.2:p.Arg1524=
ENST00000460952.1:n.149C= (STRC)
ENST00000471703.5:n.2524C= (STRC)
ENST00000485556.5:n.3425C= (STRC)
ENST00000493750.1:n.366C= (STRC)
ENST00000541030.5:c.2251C= (STRC)	ENSP00000440413.1:p.Arg751=
NM_153700.2:c.4570C= (STRC) MANE Select	NP_714544.1:p.Arg1524=
XM_011521277.1:c.5059C= (STRC)	XP_011519579.1:p.Arg1687=
XM_011521278.1:c.4675C= (STRC)	XP_011519580.1:p.Arg1559=
XM_011521279.1:c.4675C= (STRC)	XP_011519581.1:p.Arg1559=