Canonical Allele Identifier: CA2173247774

Gene: STRC CKMT1B

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43599737G= , CM000677.2:g.43599737G=	GRCh38
NC_000015.9:g.43891935G= , CM000677.1:g.43891935G=	GRCh37
NC_000015.8:g.41679227G=	NCBI36
NG_011636.1:g.24064C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.5263C= (STRC) MANE Select	ENSP00000401513.2:p.Gln1755=
ENST00000411560.1:n.142+204G= (CKMT1B)
ENST00000428650.5:c.*2296C= (STRC)	ENSP00000415991.1:n.*2296C=
ENST00000440125.5:c.*3055C= (STRC)	ENSP00000394866.1:n.*3055C=
ENST00000448437.6:n.2383C= (STRC)
ENST00000450892.6:c.5263C= (STRC)	ENSP00000401513.2:p.Gln1755=
ENST00000471703.5:n.3217C= (STRC)
ENST00000485556.5:n.4118C= (STRC)
ENST00000541030.5:c.2944C= (STRC)	ENSP00000440413.1:p.Gln982=
NM_153700.2:c.5263C= (STRC) MANE Select	NP_714544.1:p.Gln1755=
XM_011521277.1:c.5752C= (STRC)	XP_011519579.1:p.Gln1918=
XM_011521278.1:c.5368C= (STRC)	XP_011519580.1:p.Gln1790=
XM_011521279.1:c.5368C= (STRC)	XP_011519581.1:p.Gln1790=