Canonical Allele Identifier: CA392160847

Gene: STRC CKMT1B

Linked Data

• MyVariant Identifiers: chr15:g.43892844C>A (hg19) ; chr15:g.43600646C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43600646C>A , CM000677.2:g.43600646C>A	GRCh38
NC_000015.9:g.43892844C>A , CM000677.1:g.43892844C>A	GRCh37
NC_000015.8:g.41680136C>A	NCBI36
NG_011636.1:g.23155G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.4881G>T (STRC) MANE Select	ENSP00000401513.2:p.Gln1627His
ENST00000411560.1:n.142+1113C>A (CKMT1B)
ENST00000428650.5:c.*1914G>T (STRC)	ENSP00000415991.1:n.*1914G>T
ENST00000440125.5:c.*2673G>T (STRC)	ENSP00000394866.1:n.*2673G>T
ENST00000448437.6:n.2001G>T (STRC)
ENST00000450892.6:c.4881G>T (STRC)	ENSP00000401513.2:p.Gln1627His
ENST00000460952.1:n.460G>T (STRC)
ENST00000471703.5:n.2835G>T (STRC)
ENST00000485556.5:n.3736G>T (STRC)
ENST00000541030.5:c.2562G>T (STRC)	ENSP00000440413.1:p.Gln854His
NM_153700.2:c.4881G>T (STRC) MANE Select	NP_714544.1:p.Gln1627His
XM_011521277.1:c.5370G>T (STRC)	XP_011519579.1:p.Gln1790His
XM_011521278.1:c.4986G>T (STRC)	XP_011519580.1:p.Gln1662His
XM_011521279.1:c.4986G>T (STRC)	XP_011519581.1:p.Gln1662His