Canonical Allele Identifier: CA490145459

Gene: STRC CKMT1B

Linked Data

• MyVariant Identifiers: chr15:g.43893723A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43601525A>G , CM000677.2:g.43601525A>G	GRCh38
NC_000015.9:g.43893723A>G , CM000677.1:g.43893723A>G	GRCh37
NC_000015.8:g.41681015A>G	NCBI36
NG_011636.1:g.22276T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.4572T>C (STRC) MANE Select	ENSP00000401513.2:p.Arg1524=
ENST00000411560.1:n.142+1992A>G (CKMT1B)
ENST00000428650.5:c.*1605T>C (STRC)	ENSP00000415991.1:n.*1605T>C
ENST00000440125.5:c.*2364T>C (STRC)	ENSP00000394866.1:n.*2364T>C
ENST00000448437.6:n.1692T>C (STRC)
ENST00000450892.6:c.4572T>C (STRC)	ENSP00000401513.2:p.Arg1524=
ENST00000460952.1:n.151T>C (STRC)
ENST00000471703.5:n.2526T>C (STRC)
ENST00000485556.5:n.3427T>C (STRC)
ENST00000493750.1:n.368T>C (STRC)
ENST00000541030.5:c.2253T>C (STRC)	ENSP00000440413.1:p.Arg751=
NM_153700.2:c.4572T>C (STRC) MANE Select	NP_714544.1:p.Arg1524=
XM_011521277.1:c.5061T>C (STRC)	XP_011519579.1:p.Arg1687=
XM_011521278.1:c.4677T>C (STRC)	XP_011519580.1:p.Arg1559=
XM_011521279.1:c.4677T>C (STRC)	XP_011519581.1:p.Arg1559=