Canonical Allele Identifier: CA392160026

Gene: STRC CKMT1B

Linked Data

• MyVariant Identifiers: chr15:g.43892756A>T (hg19) ; chr15:g.43600558A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43600558A>T , CM000677.2:g.43600558A>T	GRCh38
NC_000015.9:g.43892756A>T , CM000677.1:g.43892756A>T	GRCh37
NC_000015.8:g.41680048A>T	NCBI36
NG_011636.1:g.23243T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000450892.7:c.4969T>A (STRC) MANE Select	ENSP00000401513.2:p.Phe1657Ile
ENST00000411560.1:n.142+1025A>T (CKMT1B)
ENST00000428650.5:c.*2002T>A (STRC)	ENSP00000415991.1:n.*2002T>A
ENST00000440125.5:c.*2761T>A (STRC)	ENSP00000394866.1:n.*2761T>A
ENST00000448437.6:n.2089T>A (STRC)
ENST00000450892.6:c.4969T>A (STRC)	ENSP00000401513.2:p.Phe1657Ile
ENST00000471703.5:n.2923T>A (STRC)
ENST00000485556.5:n.3824T>A (STRC)
ENST00000541030.5:c.2650T>A (STRC)	ENSP00000440413.1:p.Phe884Ile
NM_153700.2:c.4969T>A (STRC) MANE Select	NP_714544.1:p.Phe1657Ile
XM_011521277.1:c.5458T>A (STRC)	XP_011519579.1:p.Phe1820Ile
XM_011521278.1:c.5074T>A (STRC)	XP_011519580.1:p.Phe1692Ile
XM_011521279.1:c.5074T>A (STRC)	XP_011519581.1:p.Phe1692Ile