Canonical Allele Identifier: CA2173248599

Gene: STRC CKMT1B

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43601544C= , CM000677.2:g.43601544C=	GRCh38
NC_000015.9:g.43893742C= , CM000677.1:g.43893742C=	GRCh37
NC_000015.8:g.41681034C=	NCBI36
NG_011636.1:g.22257G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.4553G= (STRC) MANE Select	ENSP00000401513.2:p.Gly1518=
ENST00000411560.1:n.142+2011C= (CKMT1B)
ENST00000428650.5:c.*1586G= (STRC)	ENSP00000415991.1:n.*1586G=
ENST00000440125.5:c.*2345G= (STRC)	ENSP00000394866.1:n.*2345G=
ENST00000448437.6:n.1673G= (STRC)
ENST00000450892.6:c.4553G= (STRC)	ENSP00000401513.2:p.Gly1518=
ENST00000460952.1:n.132G= (STRC)
ENST00000471703.5:n.2507G= (STRC)
ENST00000485556.5:n.3408G= (STRC)
ENST00000493750.1:n.349G= (STRC)
ENST00000541030.5:c.2234G= (STRC)	ENSP00000440413.1:p.Gly745=
NM_153700.2:c.4553G= (STRC) MANE Select	NP_714544.1:p.Gly1518=
XM_011521277.1:c.5042G= (STRC)	XP_011519579.1:p.Gly1681=
XM_011521278.1:c.4658G= (STRC)	XP_011519580.1:p.Gly1553=
XM_011521279.1:c.4658G= (STRC)	XP_011519581.1:p.Gly1553=