Canonical Allele Identifier: CA2173248519

Gene: STRC CKMT1B

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43601387A= , CM000677.2:g.43601387A=	GRCh38
NC_000015.9:g.43893585A= , CM000677.1:g.43893585A=	GRCh37
NC_000015.8:g.41680877A=	NCBI36
NG_011636.1:g.22414T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.4701+9T= (STRC) MANE Select	ENSP00000401513.2:n.4701+9T=
ENST00000411560.1:n.142+1854A= (CKMT1B)
ENST00000428650.5:c.*1734+9T= (STRC)	ENSP00000415991.1:n.*1734+9T=
ENST00000440125.5:c.*2493+9T= (STRC)	ENSP00000394866.1:n.*2493+9T=
ENST00000448437.6:n.1821+9T= (STRC)
ENST00000450892.6:c.4701+9T= (STRC)	ENSP00000401513.2:n.4701+9T=
ENST00000460952.1:n.280+9T= (STRC)
ENST00000471703.5:n.2655+9T= (STRC)
ENST00000485556.5:n.3556+9T= (STRC)
ENST00000493750.1:n.497+9T= (STRC)
ENST00000541030.5:c.2382+9T= (STRC)	ENSP00000440413.1:n.2382+9T=
NM_153700.2:c.4701+9T= (STRC) MANE Select	NP_714544.1:n.4701+9T=
XM_011521277.1:c.5190+9T= (STRC)	XP_011519579.1:n.5190+9T=
XM_011521278.1:c.4806+9T= (STRC)	XP_011519580.1:n.4806+9T=
XM_011521279.1:c.4806+9T= (STRC)	XP_011519581.1:n.4806+9T=