Canonical Allele Identifier: CA2173248143

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.43600694_43600698delinsTAGGA , CM000677.2:g.43600694_43600698delinsTAGGA GRCh38
NC_000015.9:g.43892892_43892896delinsTAGGA , CM000677.1:g.43892892_43892896delinsTAGGA GRCh37
NC_000015.8:g.41680184_41680188delinsTAGGA NCBI36
NG_011636.1:g.23103_23107delinsTCCTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000450892.7:c.4845-16_4845-12delinsTCCTA (STRC) MANE Select ENSP00000401513.2:n.4845-16_4845-12delinsTCCTA
ENST00000411560.1:n.142+1161_142+1165delinsTAGGA (CKMT1B)
ENST00000428650.5:c.*1878-16_*1878-12delinsTCCTA (STRC) ENSP00000415991.1:n.*1878-16_*1878-12delinsTCCTA
ENST00000440125.5:c.*2637-16_*2637-12delinsTCCTA (STRC) ENSP00000394866.1:n.*2637-16_*2637-12delinsTCCTA
ENST00000448437.6:n.1965-16_1965-12delinsTCCTA (STRC)
ENST00000450892.6:c.4845-16_4845-12delinsTCCTA (STRC) ENSP00000401513.2:n.4845-16_4845-12delinsTCCTA
ENST00000460952.1:n.424-16_424-12delinsTCCTA (STRC)
ENST00000471703.5:n.2799-16_2799-12delinsTCCTA (STRC)
ENST00000485556.5:n.3700-16_3700-12delinsTCCTA (STRC)
ENST00000541030.5:c.2526-16_2526-12delinsTCCTA (STRC) ENSP00000440413.1:n.2526-16_2526-12delinsTCCTA
NM_153700.2:c.4845-16_4845-12delinsTCCTA (STRC) MANE Select NP_714544.1:n.4845-16_4845-12delinsTCCTA
XM_011521277.1:c.5334-16_5334-12delinsTCCTA (STRC) XP_011519579.1:n.5334-16_5334-12delinsTCCTA
XM_011521278.1:c.4950-16_4950-12delinsTCCTA (STRC) XP_011519580.1:n.4950-16_4950-12delinsTCCTA
XM_011521279.1:c.4950-16_4950-12delinsTCCTA (STRC) XP_011519581.1:n.4950-16_4950-12delinsTCCTA