Canonical Allele Identifier: CA490145321

Gene: STRC CKMT1B

Linked Data

• MyVariant Identifiers: chr15:g.43893618C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43601420C>T , CM000677.2:g.43601420C>T	GRCh38
NC_000015.9:g.43893618C>T , CM000677.1:g.43893618C>T	GRCh37
NC_000015.8:g.41680910C>T	NCBI36
NG_011636.1:g.22381G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.4677G>A (STRC) MANE Select	ENSP00000401513.2:p.Gln1559=
ENST00000411560.1:n.142+1887C>T (CKMT1B)
ENST00000428650.5:c.*1710G>A (STRC)	ENSP00000415991.1:n.*1710G>A
ENST00000440125.5:c.*2469G>A (STRC)	ENSP00000394866.1:n.*2469G>A
ENST00000448437.6:n.1797G>A (STRC)
ENST00000450892.6:c.4677G>A (STRC)	ENSP00000401513.2:p.Gln1559=
ENST00000460952.1:n.256G>A (STRC)
ENST00000471703.5:n.2631G>A (STRC)
ENST00000485556.5:n.3532G>A (STRC)
ENST00000493750.1:n.473G>A (STRC)
ENST00000541030.5:c.2358G>A (STRC)	ENSP00000440413.1:p.Gln786=
NM_153700.2:c.4677G>A (STRC) MANE Select	NP_714544.1:p.Gln1559=
XM_011521277.1:c.5166G>A (STRC)	XP_011519579.1:p.Gln1722=
XM_011521278.1:c.4782G>A (STRC)	XP_011519580.1:p.Gln1594=
XM_011521279.1:c.4782G>A (STRC)	XP_011519581.1:p.Gln1594=