Canonical Allele Identifier: CA2628142195

Gene: STRC CKMT1B

Linked Data

• gnomAD v4: 15-43601374-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43601375del , CM000677.2:g.43601375del	GRCh38
NC_000015.9:g.43893573del , CM000677.1:g.43893573del	GRCh37
NC_000015.8:g.41680865del	NCBI36
NG_011636.1:g.22426del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.4701+21del (STRC) MANE Select	ENSP00000401513.2:n.4701+21del
ENST00000411560.1:n.142+1842del (CKMT1B)
ENST00000428650.5:c.*1734+21del (STRC)	ENSP00000415991.1:n.*1734+21del
ENST00000440125.5:c.*2493+21del (STRC)	ENSP00000394866.1:n.*2493+21del
ENST00000448437.6:n.1821+21del (STRC)
ENST00000450892.6:c.4701+21del (STRC)	ENSP00000401513.2:n.4701+21del
ENST00000460952.1:n.280+21del (STRC)
ENST00000471703.5:n.2655+21del (STRC)
ENST00000485556.5:n.3556+21del (STRC)
ENST00000493750.1:n.497+21del (STRC)
ENST00000541030.5:c.2382+21del (STRC)	ENSP00000440413.1:n.2382+21del
NM_153700.2:c.4701+21del (STRC) MANE Select	NP_714544.1:n.4701+21del
XM_011521277.1:c.5190+21del (STRC)	XP_011519579.1:n.5190+21del
XM_011521278.1:c.4806+21del (STRC)	XP_011519580.1:n.4806+21del
XM_011521279.1:c.4806+21del (STRC)	XP_011519581.1:n.4806+21del