Canonical Allele Identifier: CA2173248442

Gene: STRC CKMT1B

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43601260_43601261delinsTG , CM000677.2:g.43601260_43601261delinsTG	GRCh38
NC_000015.9:g.43893458_43893459delinsTG , CM000677.1:g.43893458_43893459delinsTG	GRCh37
NC_000015.8:g.41680750_41680751delinsTG	NCBI36
NG_011636.1:g.22540_22541delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.4701+135_4701+136delinsCA (STRC) MANE Select	ENSP00000401513.2:n.4701+135_4701+136delinsCA
ENST00000411560.1:n.142+1727_142+1728delinsTG (CKMT1B)
ENST00000428650.5:c.*1734+135_*1734+136delinsCA (STRC)	ENSP00000415991.1:n.*1734+135_*1734+136delinsCA
ENST00000440125.5:c.*2493+135_*2493+136delinsCA (STRC)	ENSP00000394866.1:n.*2493+135_*2493+136delinsCA
ENST00000448437.6:n.1821+135_1821+136delinsCA (STRC)
ENST00000450892.6:c.4701+135_4701+136delinsCA (STRC)	ENSP00000401513.2:n.4701+135_4701+136delinsCA
ENST00000460952.1:n.280+135_280+136delinsCA (STRC)
ENST00000471703.5:n.2655+135_2655+136delinsCA (STRC)
ENST00000485556.5:n.3556+135_3556+136delinsCA (STRC)
ENST00000493750.1:n.497+135_497+136delinsCA (STRC)
ENST00000541030.5:c.2382+135_2382+136delinsCA (STRC)	ENSP00000440413.1:n.2382+135_2382+136delinsCA
NM_153700.2:c.4701+135_4701+136delinsCA (STRC) MANE Select	NP_714544.1:n.4701+135_4701+136delinsCA
XM_011521277.1:c.5190+135_5190+136delinsCA (STRC)	XP_011519579.1:n.5190+135_5190+136delinsCA
XM_011521278.1:c.4806+135_4806+136delinsCA (STRC)	XP_011519580.1:n.4806+135_4806+136delinsCA
XM_011521279.1:c.4806+135_4806+136delinsCA (STRC)	XP_011519581.1:n.4806+135_4806+136delinsCA