Canonical Allele Identifier: CA392163140

Gene: STRC CKMT1B

Linked Data

• MyVariant Identifiers: chr15:g.43893187A>G (hg19) ; chr15:g.43600989A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43600989A>G , CM000677.2:g.43600989A>G	GRCh38
NC_000015.9:g.43893187A>G , CM000677.1:g.43893187A>G	GRCh37
NC_000015.8:g.41680479A>G	NCBI36
NG_011636.1:g.22812T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.4727T>C (STRC) MANE Select	ENSP00000401513.2:p.Leu1576Pro
ENST00000411560.1:n.142+1456A>G (CKMT1B)
ENST00000428650.5:c.*1760T>C (STRC)	ENSP00000415991.1:n.*1760T>C
ENST00000440125.5:c.*2519T>C (STRC)	ENSP00000394866.1:n.*2519T>C
ENST00000448437.6:n.1847T>C (STRC)
ENST00000450892.6:c.4727T>C (STRC)	ENSP00000401513.2:p.Leu1576Pro
ENST00000460952.1:n.306T>C (STRC)
ENST00000471703.5:n.2681T>C (STRC)
ENST00000485556.5:n.3582T>C (STRC)
ENST00000541030.5:c.2408T>C (STRC)	ENSP00000440413.1:p.Leu803Pro
NM_153700.2:c.4727T>C (STRC) MANE Select	NP_714544.1:p.Leu1576Pro
XM_011521277.1:c.5216T>C (STRC)	XP_011519579.1:p.Leu1739Pro
XM_011521278.1:c.4832T>C (STRC)	XP_011519580.1:p.Leu1611Pro
XM_011521279.1:c.4832T>C (STRC)	XP_011519581.1:p.Leu1611Pro