Canonical Allele Identifier: CA2173248127

Gene: STRC CKMT1B

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43600658G= , CM000677.2:g.43600658G=	GRCh38
NC_000015.9:g.43892856G= , CM000677.1:g.43892856G=	GRCh37
NC_000015.8:g.41680148G=	NCBI36
NG_011636.1:g.23143C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000450892.7:c.4869C= (STRC) MANE Select	ENSP00000401513.2:p.Thr1623=
ENST00000411560.1:n.142+1125G= (CKMT1B)
ENST00000428650.5:c.*1902C= (STRC)	ENSP00000415991.1:n.*1902C=
ENST00000440125.5:c.*2661C= (STRC)	ENSP00000394866.1:n.*2661C=
ENST00000448437.6:n.1989C= (STRC)
ENST00000450892.6:c.4869C= (STRC)	ENSP00000401513.2:p.Thr1623=
ENST00000460952.1:n.448C= (STRC)
ENST00000471703.5:n.2823C= (STRC)
ENST00000485556.5:n.3724C= (STRC)
ENST00000541030.5:c.2550C= (STRC)	ENSP00000440413.1:p.Thr850=
NM_153700.2:c.4869C= (STRC) MANE Select	NP_714544.1:p.Thr1623=
XM_011521277.1:c.5358C= (STRC)	XP_011519579.1:p.Thr1786=
XM_011521278.1:c.4974C= (STRC)	XP_011519580.1:p.Thr1658=
XM_011521279.1:c.4974C= (STRC)	XP_011519581.1:p.Thr1658=