Canonical Allele Identifier: CA2173248280

Gene: STRC CKMT1B

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43600956T= , CM000677.2:g.43600956T=	GRCh38
NC_000015.9:g.43893154T= , CM000677.1:g.43893154T=	GRCh37
NC_000015.8:g.41680446T=	NCBI36
NG_011636.1:g.22845A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.4760A= (STRC) MANE Select	ENSP00000401513.2:p.Asp1587=
ENST00000411560.1:n.142+1423T= (CKMT1B)
ENST00000428650.5:c.*1793A= (STRC)	ENSP00000415991.1:n.*1793A=
ENST00000440125.5:c.*2552A= (STRC)	ENSP00000394866.1:n.*2552A=
ENST00000448437.6:n.1880A= (STRC)
ENST00000450892.6:c.4760A= (STRC)	ENSP00000401513.2:p.Asp1587=
ENST00000460952.1:n.339A= (STRC)
ENST00000471703.5:n.2714A= (STRC)
ENST00000485556.5:n.3615A= (STRC)
ENST00000541030.5:c.2441A= (STRC)	ENSP00000440413.1:p.Asp814=
NM_153700.2:c.4760A= (STRC) MANE Select	NP_714544.1:p.Asp1587=
XM_011521277.1:c.5249A= (STRC)	XP_011519579.1:p.Asp1750=
XM_011521278.1:c.4865A= (STRC)	XP_011519580.1:p.Asp1622=
XM_011521279.1:c.4865A= (STRC)	XP_011519581.1:p.Asp1622=