Canonical Allele Identifier: CA392160031

Gene: STRC CKMT1B

Linked Data

• MyVariant Identifiers: chr15:g.43892757G>C (hg19) ; chr15:g.43600559G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43600559G>C , CM000677.2:g.43600559G>C	GRCh38
NC_000015.9:g.43892757G>C , CM000677.1:g.43892757G>C	GRCh37
NC_000015.8:g.41680049G>C	NCBI36
NG_011636.1:g.23242C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000450892.7:c.4968C>G (STRC) MANE Select	ENSP00000401513.2:p.Ile1656Met
ENST00000411560.1:n.142+1026G>C (CKMT1B)
ENST00000428650.5:c.*2001C>G (STRC)	ENSP00000415991.1:n.*2001C>G
ENST00000440125.5:c.*2760C>G (STRC)	ENSP00000394866.1:n.*2760C>G
ENST00000448437.6:n.2088C>G (STRC)
ENST00000450892.6:c.4968C>G (STRC)	ENSP00000401513.2:p.Ile1656Met
ENST00000471703.5:n.2922C>G (STRC)
ENST00000485556.5:n.3823C>G (STRC)
ENST00000541030.5:c.2649C>G (STRC)	ENSP00000440413.1:p.Ile883Met
NM_153700.2:c.4968C>G (STRC) MANE Select	NP_714544.1:p.Ile1656Met
XM_011521277.1:c.5457C>G (STRC)	XP_011519579.1:p.Ile1819Met
XM_011521278.1:c.5073C>G (STRC)	XP_011519580.1:p.Ile1691Met
XM_011521279.1:c.5073C>G (STRC)	XP_011519581.1:p.Ile1691Met