Canonical Allele Identifier: CA392160569

Gene: STRC CKMT1B

Linked Data

• MyVariant Identifiers: chr15:g.43892813G>C (hg19) ; chr15:g.43600615G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43600615G>C , CM000677.2:g.43600615G>C	GRCh38
NC_000015.9:g.43892813G>C , CM000677.1:g.43892813G>C	GRCh37
NC_000015.8:g.41680105G>C	NCBI36
NG_011636.1:g.23186C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.4912C>G (STRC) MANE Select	ENSP00000401513.2:p.His1638Asp
ENST00000411560.1:n.142+1082G>C (CKMT1B)
ENST00000428650.5:c.*1945C>G (STRC)	ENSP00000415991.1:n.*1945C>G
ENST00000440125.5:c.*2704C>G (STRC)	ENSP00000394866.1:n.*2704C>G
ENST00000448437.6:n.2032C>G (STRC)
ENST00000450892.6:c.4912C>G (STRC)	ENSP00000401513.2:p.His1638Asp
ENST00000460952.1:n.491C>G (STRC)
ENST00000471703.5:n.2866C>G (STRC)
ENST00000485556.5:n.3767C>G (STRC)
ENST00000541030.5:c.2593C>G (STRC)	ENSP00000440413.1:p.His865Asp
NM_153700.2:c.4912C>G (STRC) MANE Select	NP_714544.1:p.His1638Asp
XM_011521277.1:c.5401C>G (STRC)	XP_011519579.1:p.His1801Asp
XM_011521278.1:c.5017C>G (STRC)	XP_011519580.1:p.His1673Asp
XM_011521279.1:c.5017C>G (STRC)	XP_011519581.1:p.His1673Asp