Canonical Allele Identifier: CA2173248615

Gene: STRC CKMT1B

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43601564_43601565delinsCA , CM000677.2:g.43601564_43601565delinsCA	GRCh38
NC_000015.9:g.43893762_43893763delinsCA , CM000677.1:g.43893762_43893763delinsCA	GRCh37
NC_000015.8:g.41681054_41681055delinsCA	NCBI36
NG_011636.1:g.22236_22237delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.4546-14_4546-13delinsTG (STRC) MANE Select	ENSP00000401513.2:n.4546-14_4546-13delinsTG
ENST00000411560.1:n.142+2031_142+2032delinsCA (CKMT1B)
ENST00000428650.5:c.*1579-14_*1579-13delinsTG (STRC)	ENSP00000415991.1:n.*1579-14_*1579-13delinsTG
ENST00000440125.5:c.*2338-14_*2338-13delinsTG (STRC)	ENSP00000394866.1:n.*2338-14_*2338-13delinsTG
ENST00000448437.6:n.1666-14_1666-13delinsTG (STRC)
ENST00000450892.6:c.4546-14_4546-13delinsTG (STRC)	ENSP00000401513.2:n.4546-14_4546-13delinsTG
ENST00000460952.1:n.111_112delinsTG (STRC)
ENST00000471703.5:n.2500-14_2500-13delinsTG (STRC)
ENST00000485556.5:n.3401-14_3401-13delinsTG (STRC)
ENST00000493750.1:n.342-14_342-13delinsTG (STRC)
ENST00000541030.5:c.2227-14_2227-13delinsTG (STRC)	ENSP00000440413.1:n.2227-14_2227-13delinsTG
NM_153700.2:c.4546-14_4546-13delinsTG (STRC) MANE Select	NP_714544.1:n.4546-14_4546-13delinsTG
XM_011521277.1:c.5035-14_5035-13delinsTG (STRC)	XP_011519579.1:n.5035-14_5035-13delinsTG
XM_011521278.1:c.4651-14_4651-13delinsTG (STRC)	XP_011519580.1:n.4651-14_4651-13delinsTG
XM_011521279.1:c.4651-14_4651-13delinsTG (STRC)	XP_011519581.1:n.4651-14_4651-13delinsTG