Canonical Allele Identifier: CA392162561

Gene: STRC CKMT1B

Linked Data

• MyVariant Identifiers: chr15:g.43893078C>A (hg19) ; chr15:g.43600880C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43600880C>A , CM000677.2:g.43600880C>A	GRCh38
NC_000015.9:g.43893078C>A , CM000677.1:g.43893078C>A	GRCh37
NC_000015.8:g.41680370C>A	NCBI36
NG_011636.1:g.22921G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.4836G>T (STRC) MANE Select	ENSP00000401513.2:p.Trp1612Cys
ENST00000411560.1:n.142+1347C>A (CKMT1B)
ENST00000428650.5:c.*1869G>T (STRC)	ENSP00000415991.1:n.*1869G>T
ENST00000440125.5:c.*2628G>T (STRC)	ENSP00000394866.1:n.*2628G>T
ENST00000448437.6:n.1956G>T (STRC)
ENST00000450892.6:c.4836G>T (STRC)	ENSP00000401513.2:p.Trp1612Cys
ENST00000460952.1:n.415G>T (STRC)
ENST00000471703.5:n.2790G>T (STRC)
ENST00000485556.5:n.3691G>T (STRC)
ENST00000541030.5:c.2517G>T (STRC)	ENSP00000440413.1:p.Trp839Cys
NM_153700.2:c.4836G>T (STRC) MANE Select	NP_714544.1:p.Trp1612Cys
XM_011521277.1:c.5325G>T (STRC)	XP_011519579.1:p.Trp1775Cys
XM_011521278.1:c.4941G>T (STRC)	XP_011519580.1:p.Trp1647Cys
XM_011521279.1:c.4941G>T (STRC)	XP_011519581.1:p.Trp1647Cys