Canonical Allele Identifier: CA2173248626

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.43601581_43601582delinsGA , CM000677.2:g.43601581_43601582delinsGA GRCh38
NC_000015.9:g.43893779_43893780delinsGA , CM000677.1:g.43893779_43893780delinsGA GRCh37
NC_000015.8:g.41681071_41681072delinsGA NCBI36
NG_011636.1:g.22219_22220delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000450892.7:c.4546-31_4546-30delinsTC (STRC) MANE Select ENSP00000401513.2:n.4546-31_4546-30delinsTC
ENST00000411560.1:n.142+2048_142+2049delinsGA (CKMT1B)
ENST00000428650.5:c.*1579-31_*1579-30delinsTC (STRC) ENSP00000415991.1:n.*1579-31_*1579-30delinsTC
ENST00000440125.5:c.*2338-31_*2338-30delinsTC (STRC) ENSP00000394866.1:n.*2338-31_*2338-30delinsTC
ENST00000448437.6:n.1666-31_1666-30delinsTC (STRC)
ENST00000450892.6:c.4546-31_4546-30delinsTC (STRC) ENSP00000401513.2:n.4546-31_4546-30delinsTC
ENST00000460952.1:n.94_95delinsTC (STRC)
ENST00000471703.5:n.2500-31_2500-30delinsTC (STRC)
ENST00000485556.5:n.3401-31_3401-30delinsTC (STRC)
ENST00000493750.1:n.342-31_342-30delinsTC (STRC)
ENST00000541030.5:c.2227-31_2227-30delinsTC (STRC) ENSP00000440413.1:n.2227-31_2227-30delinsTC
NM_153700.2:c.4546-31_4546-30delinsTC (STRC) MANE Select NP_714544.1:n.4546-31_4546-30delinsTC
XM_011521277.1:c.5035-31_5035-30delinsTC (STRC) XP_011519579.1:n.5035-31_5035-30delinsTC
XM_011521278.1:c.4651-31_4651-30delinsTC (STRC) XP_011519580.1:n.4651-31_4651-30delinsTC
XM_011521279.1:c.4651-31_4651-30delinsTC (STRC) XP_011519581.1:n.4651-31_4651-30delinsTC