Canonical Allele Identifier: CA2173248603

Gene: STRC CKMT1B

Linked Data

• dbSNP Id: rs2085668934
• gnomAD v4: 15-43601547-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43601548del , CM000677.2:g.43601548del	GRCh38
NC_000015.9:g.43893746del , CM000677.1:g.43893746del	GRCh37
NC_000015.8:g.41681038del	NCBI36
NG_011636.1:g.22253del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.4549del (STRC) MANE Select	ENSP00000401513.2:p.Trp1517GlyfsTer19
ENST00000411560.1:n.142+2015del (CKMT1B)
ENST00000428650.5:c.*1582del (STRC)	ENSP00000415991.1:n.*1582del
ENST00000440125.5:c.*2341del (STRC)	ENSP00000394866.1:n.*2341del
ENST00000448437.6:n.1669del (STRC)
ENST00000450892.6:c.4549del (STRC)	ENSP00000401513.2:p.Trp1517GlyfsTer19
ENST00000460952.1:n.128del (STRC)
ENST00000471703.5:n.2503del (STRC)
ENST00000485556.5:n.3404del (STRC)
ENST00000493750.1:n.345del (STRC)
ENST00000541030.5:c.2230del (STRC)	ENSP00000440413.1:p.Trp744GlyfsTer19
NM_153700.2:c.4549del (STRC) MANE Select	NP_714544.1:p.Trp1517GlyfsTer19
XM_011521277.1:c.5038del (STRC)	XP_011519579.1:p.Trp1680GlyfsTer19
XM_011521278.1:c.4654del (STRC)	XP_011519580.1:p.Trp1552GlyfsTer19
XM_011521279.1:c.4654del (STRC)	XP_011519581.1:p.Trp1552GlyfsTer19