Canonical Allele Identifier: CA2173248570

Gene: STRC CKMT1B

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43601489T= , CM000677.2:g.43601489T=	GRCh38
NC_000015.9:g.43893687T= , CM000677.1:g.43893687T=	GRCh37
NC_000015.8:g.41680979T=	NCBI36
NG_011636.1:g.22312A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.4608A= (STRC) MANE Select	ENSP00000401513.2:p.Ile1536=
ENST00000411560.1:n.142+1956T= (CKMT1B)
ENST00000428650.5:c.*1641A= (STRC)	ENSP00000415991.1:n.*1641A=
ENST00000440125.5:c.*2400A= (STRC)	ENSP00000394866.1:n.*2400A=
ENST00000448437.6:n.1728A= (STRC)
ENST00000450892.6:c.4608A= (STRC)	ENSP00000401513.2:p.Ile1536=
ENST00000460952.1:n.187A= (STRC)
ENST00000471703.5:n.2562A= (STRC)
ENST00000485556.5:n.3463A= (STRC)
ENST00000493750.1:n.404A= (STRC)
ENST00000541030.5:c.2289A= (STRC)	ENSP00000440413.1:p.Ile763=
NM_153700.2:c.4608A= (STRC) MANE Select	NP_714544.1:p.Ile1536=
XM_011521277.1:c.5097A= (STRC)	XP_011519579.1:p.Ile1699=
XM_011521278.1:c.4713A= (STRC)	XP_011519580.1:p.Ile1571=
XM_011521279.1:c.4713A= (STRC)	XP_011519581.1:p.Ile1571=