Canonical Allele Identifier: CA490145305

Gene: STRC CKMT1B

Linked Data

• gnomAD v4: 15-43601399-A-C
• MyVariant Identifiers: chr15:g.43893597A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43601399A>C , CM000677.2:g.43601399A>C	GRCh38
NC_000015.9:g.43893597A>C , CM000677.1:g.43893597A>C	GRCh37
NC_000015.8:g.41680889A>C	NCBI36
NG_011636.1:g.22402T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.4698T>G (STRC) MANE Select	ENSP00000401513.2:p.Thr1566=
ENST00000411560.1:n.142+1866A>C (CKMT1B)
ENST00000428650.5:c.*1731T>G (STRC)	ENSP00000415991.1:n.*1731T>G
ENST00000440125.5:c.*2490T>G (STRC)	ENSP00000394866.1:n.*2490T>G
ENST00000448437.6:n.1818T>G (STRC)
ENST00000450892.6:c.4698T>G (STRC)	ENSP00000401513.2:p.Thr1566=
ENST00000460952.1:n.277T>G (STRC)
ENST00000471703.5:n.2652T>G (STRC)
ENST00000485556.5:n.3553T>G (STRC)
ENST00000493750.1:n.494T>G (STRC)
ENST00000541030.5:c.2379T>G (STRC)	ENSP00000440413.1:p.Thr793=
NM_153700.2:c.4698T>G (STRC) MANE Select	NP_714544.1:p.Thr1566=
XM_011521277.1:c.5187T>G (STRC)	XP_011519579.1:p.Thr1729=
XM_011521278.1:c.4803T>G (STRC)	XP_011519580.1:p.Thr1601=
XM_011521279.1:c.4803T>G (STRC)	XP_011519581.1:p.Thr1601=