Canonical Allele Identifier: CA392160693

Gene: STRC CKMT1B

Linked Data

• MyVariant Identifiers: chr15:g.43892828G>T (hg19) ; chr15:g.43600630G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43600630G>T , CM000677.2:g.43600630G>T	GRCh38
NC_000015.9:g.43892828G>T , CM000677.1:g.43892828G>T	GRCh37
NC_000015.8:g.41680120G>T	NCBI36
NG_011636.1:g.23171C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.4897C>A (STRC) MANE Select	ENSP00000401513.2:p.Leu1633Met
ENST00000411560.1:n.142+1097G>T (CKMT1B)
ENST00000428650.5:c.*1930C>A (STRC)	ENSP00000415991.1:n.*1930C>A
ENST00000440125.5:c.*2689C>A (STRC)	ENSP00000394866.1:n.*2689C>A
ENST00000448437.6:n.2017C>A (STRC)
ENST00000450892.6:c.4897C>A (STRC)	ENSP00000401513.2:p.Leu1633Met
ENST00000460952.1:n.476C>A (STRC)
ENST00000471703.5:n.2851C>A (STRC)
ENST00000485556.5:n.3752C>A (STRC)
ENST00000541030.5:c.2578C>A (STRC)	ENSP00000440413.1:p.Leu860Met
NM_153700.2:c.4897C>A (STRC) MANE Select	NP_714544.1:p.Leu1633Met
XM_011521277.1:c.5386C>A (STRC)	XP_011519579.1:p.Leu1796Met
XM_011521278.1:c.5002C>A (STRC)	XP_011519580.1:p.Leu1668Met
XM_011521279.1:c.5002C>A (STRC)	XP_011519581.1:p.Leu1668Met