Canonical Allele Identifier: CA392160487

Gene: STRC CKMT1B

Linked Data

• MyVariant Identifiers: chr15:g.43892803A>T (hg19) ; chr15:g.43600605A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43600605A>T , CM000677.2:g.43600605A>T	GRCh38
NC_000015.9:g.43892803A>T , CM000677.1:g.43892803A>T	GRCh37
NC_000015.8:g.41680095A>T	NCBI36
NG_011636.1:g.23196T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.4922T>A (STRC) MANE Select	ENSP00000401513.2:p.Val1641Glu
ENST00000411560.1:n.142+1072A>T (CKMT1B)
ENST00000428650.5:c.*1955T>A (STRC)	ENSP00000415991.1:n.*1955T>A
ENST00000440125.5:c.*2714T>A (STRC)	ENSP00000394866.1:n.*2714T>A
ENST00000448437.6:n.2042T>A (STRC)
ENST00000450892.6:c.4922T>A (STRC)	ENSP00000401513.2:p.Val1641Glu
ENST00000460952.1:n.501T>A (STRC)
ENST00000471703.5:n.2876T>A (STRC)
ENST00000485556.5:n.3777T>A (STRC)
ENST00000541030.5:c.2603T>A (STRC)	ENSP00000440413.1:p.Val868Glu
NM_153700.2:c.4922T>A (STRC) MANE Select	NP_714544.1:p.Val1641Glu
XM_011521277.1:c.5411T>A (STRC)	XP_011519579.1:p.Val1804Glu
XM_011521278.1:c.5027T>A (STRC)	XP_011519580.1:p.Val1676Glu
XM_011521279.1:c.5027T>A (STRC)	XP_011519581.1:p.Val1676Glu