Canonical Allele Identifier: CA2173251906

Gene: STRC CKMT1B

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43604375A= , CM000677.2:g.43604375A=	GRCh38
NC_000015.9:g.43896573A= , CM000677.1:g.43896573A=	GRCh37
NC_000015.8:g.41683865A=	NCBI36
NG_011636.1:g.19426T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.4204T= (STRC) MANE Select	ENSP00000401513.2:p.Ser1402=
ENST00000411560.1:n.143-409A= (CKMT1B)
ENST00000428650.5:c.*1407T= (STRC)	ENSP00000415991.1:n.*1407T=
ENST00000440125.5:c.*1996T= (STRC)	ENSP00000394866.1:n.*1996T=
ENST00000448437.6:n.1666-2824T= (STRC)
ENST00000450892.6:c.4204T= (STRC)	ENSP00000401513.2:p.Ser1402=
ENST00000471703.5:n.2158T= (STRC)
ENST00000485556.5:n.3059T= (STRC)
ENST00000541030.5:c.1885T= (STRC)	ENSP00000440413.1:p.Ser629=
NM_153700.2:c.4204T= (STRC) MANE Select	NP_714544.1:p.Ser1402=
XM_011521277.1:c.4693T= (STRC)	XP_011519579.1:p.Ser1565=
XM_011521278.1:c.4309T= (STRC)	XP_011519580.1:p.Ser1437=
XM_011521279.1:c.4309T= (STRC)	XP_011519581.1:p.Ser1437=