Canonical Allele Identifier: CA490145378

Gene: STRC CKMT1B

Linked Data

• dbSNP Id: rs2085667827
• MyVariant Identifiers: chr15:g.43893660C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43601462C>T , CM000677.2:g.43601462C>T	GRCh38
NC_000015.9:g.43893660C>T , CM000677.1:g.43893660C>T	GRCh37
NC_000015.8:g.41680952C>T	NCBI36
NG_011636.1:g.22339G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.4635G>A (STRC) MANE Select	ENSP00000401513.2:p.Glu1545=
ENST00000411560.1:n.142+1929C>T (CKMT1B)
ENST00000428650.5:c.*1668G>A (STRC)	ENSP00000415991.1:n.*1668G>A
ENST00000440125.5:c.*2427G>A (STRC)	ENSP00000394866.1:n.*2427G>A
ENST00000448437.6:n.1755G>A (STRC)
ENST00000450892.6:c.4635G>A (STRC)	ENSP00000401513.2:p.Glu1545=
ENST00000460952.1:n.214G>A (STRC)
ENST00000471703.5:n.2589G>A (STRC)
ENST00000485556.5:n.3490G>A (STRC)
ENST00000493750.1:n.431G>A (STRC)
ENST00000541030.5:c.2316G>A (STRC)	ENSP00000440413.1:p.Glu772=
NM_153700.2:c.4635G>A (STRC) MANE Select	NP_714544.1:p.Glu1545=
XM_011521277.1:c.5124G>A (STRC)	XP_011519579.1:p.Glu1708=
XM_011521278.1:c.4740G>A (STRC)	XP_011519580.1:p.Glu1580=
XM_011521279.1:c.4740G>A (STRC)	XP_011519581.1:p.Glu1580=