Canonical Allele Identifier: CA490145486

Gene: STRC CKMT1B

Linked Data

• COSMIC: COSM6046090
• MyVariant Identifiers: chr15:g.43893741A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43601543A>G , CM000677.2:g.43601543A>G	GRCh38
NC_000015.9:g.43893741A>G , CM000677.1:g.43893741A>G	GRCh37
NC_000015.8:g.41681033A>G	NCBI36
NG_011636.1:g.22258T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.4554T>C (STRC) MANE Select	ENSP00000401513.2:p.Gly1518=
ENST00000411560.1:n.142+2010A>G (CKMT1B)
ENST00000428650.5:c.*1587T>C (STRC)	ENSP00000415991.1:n.*1587T>C
ENST00000440125.5:c.*2346T>C (STRC)	ENSP00000394866.1:n.*2346T>C
ENST00000448437.6:n.1674T>C (STRC)
ENST00000450892.6:c.4554T>C (STRC)	ENSP00000401513.2:p.Gly1518=
ENST00000460952.1:n.133T>C (STRC)
ENST00000471703.5:n.2508T>C (STRC)
ENST00000485556.5:n.3409T>C (STRC)
ENST00000493750.1:n.350T>C (STRC)
ENST00000541030.5:c.2235T>C (STRC)	ENSP00000440413.1:p.Gly745=
NM_153700.2:c.4554T>C (STRC) MANE Select	NP_714544.1:p.Gly1518=
XM_011521277.1:c.5043T>C (STRC)	XP_011519579.1:p.Gly1681=
XM_011521278.1:c.4659T>C (STRC)	XP_011519580.1:p.Gly1553=
XM_011521279.1:c.4659T>C (STRC)	XP_011519581.1:p.Gly1553=