Canonical Allele Identifier: CA2575704370

Gene: STRC CKMT1B

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43601607T>G , CM000677.2:g.43601607T>G	GRCh38
NC_000015.9:g.43893805T>G , CM000677.1:g.43893805T>G	GRCh37
NC_000015.8:g.41681097T>G	NCBI36
NG_011636.1:g.22194A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.4546-56A>C (STRC) MANE Select	ENSP00000401513.2:n.4546-56A>C
ENST00000411560.1:n.142+2074T>G (CKMT1B)
ENST00000428650.5:c.*1579-56A>C (STRC)	ENSP00000415991.1:n.*1579-56A>C
ENST00000440125.5:c.*2338-56A>C (STRC)	ENSP00000394866.1:n.*2338-56A>C
ENST00000448437.6:n.1666-56A>C (STRC)
ENST00000450892.6:c.4546-56A>C (STRC)	ENSP00000401513.2:n.4546-56A>C
ENST00000460952.1:n.69A>C (STRC)
ENST00000471703.5:n.2500-56A>C (STRC)
ENST00000485556.5:n.3401-56A>C (STRC)
ENST00000493750.1:n.342-56A>C (STRC)
ENST00000541030.5:c.2227-56A>C (STRC)	ENSP00000440413.1:n.2227-56A>C
NM_153700.2:c.4546-56A>C (STRC) MANE Select	NP_714544.1:n.4546-56A>C
XM_011521277.1:c.5035-56A>C (STRC)	XP_011519579.1:n.5035-56A>C
XM_011521278.1:c.4651-56A>C (STRC)	XP_011519580.1:n.4651-56A>C
XM_011521279.1:c.4651-56A>C (STRC)	XP_011519581.1:n.4651-56A>C