Canonical Allele Identifier: CA2839758405

Gene: STRC CKMT1B

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43601569dup , CM000677.2:g.43601569dup	GRCh38
NC_000015.9:g.43893767dup , CM000677.1:g.43893767dup	GRCh37
NC_000015.8:g.41681059dup	NCBI36
NG_011636.1:g.22233dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.4546-17dup (STRC) MANE Select	ENSP00000401513.2:n.4546-17dup
ENST00000411560.1:n.142+2036dup (CKMT1B)
ENST00000428650.5:c.*1579-17dup (STRC)	ENSP00000415991.1:n.*1579-17dup
ENST00000440125.5:c.*2338-17dup (STRC)	ENSP00000394866.1:n.*2338-17dup
ENST00000448437.6:n.1666-17dup (STRC)
ENST00000450892.6:c.4546-17dup (STRC)	ENSP00000401513.2:n.4546-17dup
ENST00000460952.1:n.108dup (STRC)
ENST00000471703.5:n.2500-17dup (STRC)
ENST00000485556.5:n.3401-17dup (STRC)
ENST00000493750.1:n.342-17dup (STRC)
ENST00000541030.5:c.2227-17dup (STRC)	ENSP00000440413.1:n.2227-17dup
NM_153700.2:c.4546-17dup (STRC) MANE Select	NP_714544.1:n.4546-17dup
XM_011521277.1:c.5035-17dup (STRC)	XP_011519579.1:n.5035-17dup
XM_011521278.1:c.4651-17dup (STRC)	XP_011519580.1:n.4651-17dup
XM_011521279.1:c.4651-17dup (STRC)	XP_011519581.1:n.4651-17dup