Canonical Allele Identifier: CA2173248459

Gene: STRC CKMT1B

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43601289_43601290delinsAC , CM000677.2:g.43601289_43601290delinsAC	GRCh38
NC_000015.9:g.43893487_43893488delinsAC , CM000677.1:g.43893487_43893488delinsAC	GRCh37
NC_000015.8:g.41680779_41680780delinsAC	NCBI36
NG_011636.1:g.22511_22512delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.4701+106_4701+107delinsGT (STRC) MANE Select	ENSP00000401513.2:n.4701+106_4701+107delinsGT
ENST00000411560.1:n.142+1756_142+1757delinsAC (CKMT1B)
ENST00000428650.5:c.*1734+106_*1734+107delinsGT (STRC)	ENSP00000415991.1:n.*1734+106_*1734+107delinsGT
ENST00000440125.5:c.*2493+106_*2493+107delinsGT (STRC)	ENSP00000394866.1:n.*2493+106_*2493+107delinsGT
ENST00000448437.6:n.1821+106_1821+107delinsGT (STRC)
ENST00000450892.6:c.4701+106_4701+107delinsGT (STRC)	ENSP00000401513.2:n.4701+106_4701+107delinsGT
ENST00000460952.1:n.280+106_280+107delinsGT (STRC)
ENST00000471703.5:n.2655+106_2655+107delinsGT (STRC)
ENST00000485556.5:n.3556+106_3556+107delinsGT (STRC)
ENST00000493750.1:n.497+106_497+107delinsGT (STRC)
ENST00000541030.5:c.2382+106_2382+107delinsGT (STRC)	ENSP00000440413.1:n.2382+106_2382+107delinsGT
NM_153700.2:c.4701+106_4701+107delinsGT (STRC) MANE Select	NP_714544.1:n.4701+106_4701+107delinsGT
XM_011521277.1:c.5190+106_5190+107delinsGT (STRC)	XP_011519579.1:n.5190+106_5190+107delinsGT
XM_011521278.1:c.4806+106_4806+107delinsGT (STRC)	XP_011519580.1:n.4806+106_4806+107delinsGT
XM_011521279.1:c.4806+106_4806+107delinsGT (STRC)	XP_011519581.1:n.4806+106_4806+107delinsGT