Canonical Allele Identifier: CA392157882

Gene: STRC CKMT1B

Linked Data

• MyVariant Identifiers: chr15:g.43892160T>A (hg19) ; chr15:g.43599962T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43599962T>A , CM000677.2:g.43599962T>A	GRCh38
NC_000015.9:g.43892160T>A , CM000677.1:g.43892160T>A	GRCh37
NC_000015.8:g.41679452T>A	NCBI36
NG_011636.1:g.23839A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.5237A>T (STRC) MANE Select	ENSP00000401513.2:p.Gln1746Leu
ENST00000411560.1:n.142+429T>A (CKMT1B)
ENST00000428650.5:c.*2270A>T (STRC)	ENSP00000415991.1:n.*2270A>T
ENST00000440125.5:c.*3029A>T (STRC)	ENSP00000394866.1:n.*3029A>T
ENST00000448437.6:n.2357A>T (STRC)
ENST00000450892.6:c.5237A>T (STRC)	ENSP00000401513.2:p.Gln1746Leu
ENST00000471703.5:n.3191A>T (STRC)
ENST00000485556.5:n.4092A>T (STRC)
ENST00000541030.5:c.2918A>T (STRC)	ENSP00000440413.1:p.Gln973Leu
NM_153700.2:c.5237A>T (STRC) MANE Select	NP_714544.1:p.Gln1746Leu
XM_011521277.1:c.5726A>T (STRC)	XP_011519579.1:p.Gln1909Leu
XM_011521278.1:c.5342A>T (STRC)	XP_011519580.1:p.Gln1781Leu
XM_011521279.1:c.5342A>T (STRC)	XP_011519581.1:p.Gln1781Leu