Canonical Allele Identifier: CA490145347

Gene: STRC CKMT1B

Linked Data

• MyVariant Identifiers: chr15:g.43893636C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43601438C>A , CM000677.2:g.43601438C>A	GRCh38
NC_000015.9:g.43893636C>A , CM000677.1:g.43893636C>A	GRCh37
NC_000015.8:g.41680928C>A	NCBI36
NG_011636.1:g.22363G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.4659G>T (STRC) MANE Select	ENSP00000401513.2:p.Val1553=
ENST00000411560.1:n.142+1905C>A (CKMT1B)
ENST00000428650.5:c.*1692G>T (STRC)	ENSP00000415991.1:n.*1692G>T
ENST00000440125.5:c.*2451G>T (STRC)	ENSP00000394866.1:n.*2451G>T
ENST00000448437.6:n.1779G>T (STRC)
ENST00000450892.6:c.4659G>T (STRC)	ENSP00000401513.2:p.Val1553=
ENST00000460952.1:n.238G>T (STRC)
ENST00000471703.5:n.2613G>T (STRC)
ENST00000485556.5:n.3514G>T (STRC)
ENST00000493750.1:n.455G>T (STRC)
ENST00000541030.5:c.2340G>T (STRC)	ENSP00000440413.1:p.Val780=
NM_153700.2:c.4659G>T (STRC) MANE Select	NP_714544.1:p.Val1553=
XM_011521277.1:c.5148G>T (STRC)	XP_011519579.1:p.Val1716=
XM_011521278.1:c.4764G>T (STRC)	XP_011519580.1:p.Val1588=
XM_011521279.1:c.4764G>T (STRC)	XP_011519581.1:p.Val1588=