Canonical Allele Identifier: CA2173248564

Gene: STRC CKMT1B

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43601480_43601481delinsTC , CM000677.2:g.43601480_43601481delinsTC	GRCh38
NC_000015.9:g.43893678_43893679delinsTC , CM000677.1:g.43893678_43893679delinsTC	GRCh37
NC_000015.8:g.41680970_41680971delinsTC	NCBI36
NG_011636.1:g.22320_22321delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.4616_4617delinsGA (STRC) MANE Select	ENSP00000401513.2:p.Gly1539=
ENST00000411560.1:n.142+1947_142+1948delinsTC (CKMT1B)
ENST00000428650.5:c.*1649_*1650delinsGA (STRC)	ENSP00000415991.1:n.*1649_*1650delinsGA
ENST00000440125.5:c.*2408_*2409delinsGA (STRC)	ENSP00000394866.1:n.*2408_*2409delinsGA
ENST00000448437.6:n.1736_1737delinsGA (STRC)
ENST00000450892.6:c.4616_4617delinsGA (STRC)	ENSP00000401513.2:p.Gly1539=
ENST00000460952.1:n.195_196delinsGA (STRC)
ENST00000471703.5:n.2570_2571delinsGA (STRC)
ENST00000485556.5:n.3471_3472delinsGA (STRC)
ENST00000493750.1:n.412_413delinsGA (STRC)
ENST00000541030.5:c.2297_2298delinsGA (STRC)	ENSP00000440413.1:p.Gly766=
NM_153700.2:c.4616_4617delinsGA (STRC) MANE Select	NP_714544.1:p.Gly1539=
XM_011521277.1:c.5105_5106delinsGA (STRC)	XP_011519579.1:p.Gly1702=
XM_011521278.1:c.4721_4722delinsGA (STRC)	XP_011519580.1:p.Gly1574=
XM_011521279.1:c.4721_4722delinsGA (STRC)	XP_011519581.1:p.Gly1574=