Canonical Allele Identifier: CA2628140924
Gene: STRC HGNC NCBI
CKMT1B HGNC NCBI

Linked Data

gnomAD v4: 15-43604283-CT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.43604286del , CM000677.2:g.43604286del GRCh38
NC_000015.9:g.43896484del , CM000677.1:g.43896484del GRCh37
NC_000015.8:g.41683776del NCBI36
NG_011636.1:g.19517del

Transcript Alleles

HGVS Amino-acid Change
ENST00000450892.7:c.4218+77del (STRC) MANE Select ENSP00000401513.2:n.4218+77del
ENST00000411560.1:n.143-498del (CKMT1B)
ENST00000428650.5:c.*1421+77del (STRC) ENSP00000415991.1:n.*1421+77del
ENST00000440125.5:c.*2010+77del (STRC) ENSP00000394866.1:n.*2010+77del
ENST00000448437.6:n.1666-2733del (STRC)
ENST00000450892.6:c.4218+77del (STRC) ENSP00000401513.2:n.4218+77del
ENST00000471703.5:n.2172+77del (STRC)
ENST00000485556.5:n.3073+77del (STRC)
ENST00000541030.5:c.1899+77del (STRC) ENSP00000440413.1:n.1899+77del
NM_153700.2:c.4218+77del (STRC) MANE Select NP_714544.1:n.4218+77del
XM_011521277.1:c.4707+77del (STRC) XP_011519579.1:n.4707+77del
XM_011521278.1:c.4323+77del (STRC) XP_011519580.1:n.4323+77del
XM_011521279.1:c.4323+77del (STRC) XP_011519581.1:n.4323+77del
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