Canonical Allele Identifier: CA392157938

Gene: STRC CKMT1B

Linked Data

• MyVariant Identifiers: chr15:g.43892165T>G (hg19) ; chr15:g.43599967T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43599967T>G , CM000677.2:g.43599967T>G	GRCh38
NC_000015.9:g.43892165T>G , CM000677.1:g.43892165T>G	GRCh37
NC_000015.8:g.41679457T>G	NCBI36
NG_011636.1:g.23834A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.5232A>C (STRC) MANE Select	ENSP00000401513.2:p.Glu1744Asp
ENST00000411560.1:n.142+434T>G (CKMT1B)
ENST00000428650.5:c.*2265A>C (STRC)	ENSP00000415991.1:n.*2265A>C
ENST00000440125.5:c.*3024A>C (STRC)	ENSP00000394866.1:n.*3024A>C
ENST00000448437.6:n.2352A>C (STRC)
ENST00000450892.6:c.5232A>C (STRC)	ENSP00000401513.2:p.Glu1744Asp
ENST00000471703.5:n.3186A>C (STRC)
ENST00000485556.5:n.4087A>C (STRC)
ENST00000541030.5:c.2913A>C (STRC)	ENSP00000440413.1:p.Glu971Asp
NM_153700.2:c.5232A>C (STRC) MANE Select	NP_714544.1:p.Glu1744Asp
XM_011521277.1:c.5721A>C (STRC)	XP_011519579.1:p.Glu1907Asp
XM_011521278.1:c.5337A>C (STRC)	XP_011519580.1:p.Glu1779Asp
XM_011521279.1:c.5337A>C (STRC)	XP_011519581.1:p.Glu1779Asp