Canonical Allele Identifier: CA2173247836

Gene: STRC CKMT1B

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43599931_43599932delinsAG , CM000677.2:g.43599931_43599932delinsAG	GRCh38
NC_000015.9:g.43892129_43892130delinsAG , CM000677.1:g.43892129_43892130delinsAG	GRCh37
NC_000015.8:g.41679421_41679422delinsAG	NCBI36
NG_011636.1:g.23869_23870delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.5239+28_5239+29delinsCT (STRC) MANE Select	ENSP00000401513.2:n.5239+28_5239+29delinsCT
ENST00000411560.1:n.142+398_142+399delinsAG (CKMT1B)
ENST00000428650.5:c.*2272+28_*2272+29delinsCT (STRC)	ENSP00000415991.1:n.*2272+28_*2272+29delinsCT
ENST00000440125.5:c.*3031+28_*3031+29delinsCT (STRC)	ENSP00000394866.1:n.*3031+28_*3031+29delinsCT
ENST00000448437.6:n.2359+28_2359+29delinsCT (STRC)
ENST00000450892.6:c.5239+28_5239+29delinsCT (STRC)	ENSP00000401513.2:n.5239+28_5239+29delinsCT
ENST00000471703.5:n.3193+28_3193+29delinsCT (STRC)
ENST00000485556.5:n.4094+28_4094+29delinsCT (STRC)
ENST00000541030.5:c.2920+28_2920+29delinsCT (STRC)	ENSP00000440413.1:n.2920+28_2920+29delinsCT
NM_153700.2:c.5239+28_5239+29delinsCT (STRC) MANE Select	NP_714544.1:n.5239+28_5239+29delinsCT
XM_011521277.1:c.5728+28_5728+29delinsCT (STRC)	XP_011519579.1:n.5728+28_5728+29delinsCT
XM_011521278.1:c.5344+28_5344+29delinsCT (STRC)	XP_011519580.1:n.5344+28_5344+29delinsCT
XM_011521279.1:c.5344+28_5344+29delinsCT (STRC)	XP_011519581.1:n.5344+28_5344+29delinsCT