Canonical Allele Identifier: CA2173248547

Gene: STRC CKMT1B

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43601445C= , CM000677.2:g.43601445C=	GRCh38
NC_000015.9:g.43893643C= , CM000677.1:g.43893643C=	GRCh37
NC_000015.8:g.41680935C=	NCBI36
NG_011636.1:g.22356G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.4652G= (STRC) MANE Select	ENSP00000401513.2:p.Trp1551=
ENST00000411560.1:n.142+1912C= (CKMT1B)
ENST00000428650.5:c.*1685G= (STRC)	ENSP00000415991.1:n.*1685G=
ENST00000440125.5:c.*2444G= (STRC)	ENSP00000394866.1:n.*2444G=
ENST00000448437.6:n.1772G= (STRC)
ENST00000450892.6:c.4652G= (STRC)	ENSP00000401513.2:p.Trp1551=
ENST00000460952.1:n.231G= (STRC)
ENST00000471703.5:n.2606G= (STRC)
ENST00000485556.5:n.3507G= (STRC)
ENST00000493750.1:n.448G= (STRC)
ENST00000541030.5:c.2333G= (STRC)	ENSP00000440413.1:p.Trp778=
NM_153700.2:c.4652G= (STRC) MANE Select	NP_714544.1:p.Trp1551=
XM_011521277.1:c.5141G= (STRC)	XP_011519579.1:p.Trp1714=
XM_011521278.1:c.4757G= (STRC)	XP_011519580.1:p.Trp1586=
XM_011521279.1:c.4757G= (STRC)	XP_011519581.1:p.Trp1586=