Canonical Allele Identifier: CA392160532

Gene: STRC CKMT1B

Linked Data

• MyVariant Identifiers: chr15:g.43892809A>C (hg19) ; chr15:g.43600611A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43600611A>C , CM000677.2:g.43600611A>C	GRCh38
NC_000015.9:g.43892809A>C , CM000677.1:g.43892809A>C	GRCh37
NC_000015.8:g.41680101A>C	NCBI36
NG_011636.1:g.23190T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.4916T>G (STRC) MANE Select	ENSP00000401513.2:p.Leu1639Arg
ENST00000411560.1:n.142+1078A>C (CKMT1B)
ENST00000428650.5:c.*1949T>G (STRC)	ENSP00000415991.1:n.*1949T>G
ENST00000440125.5:c.*2708T>G (STRC)	ENSP00000394866.1:n.*2708T>G
ENST00000448437.6:n.2036T>G (STRC)
ENST00000450892.6:c.4916T>G (STRC)	ENSP00000401513.2:p.Leu1639Arg
ENST00000460952.1:n.495T>G (STRC)
ENST00000471703.5:n.2870T>G (STRC)
ENST00000485556.5:n.3771T>G (STRC)
ENST00000541030.5:c.2597T>G (STRC)	ENSP00000440413.1:p.Leu866Arg
NM_153700.2:c.4916T>G (STRC) MANE Select	NP_714544.1:p.Leu1639Arg
XM_011521277.1:c.5405T>G (STRC)	XP_011519579.1:p.Leu1802Arg
XM_011521278.1:c.5021T>G (STRC)	XP_011519580.1:p.Leu1674Arg
XM_011521279.1:c.5021T>G (STRC)	XP_011519581.1:p.Leu1674Arg