Canonical Allele Identifier: CA2173247759

Gene: STRC CKMT1B

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43599668A= , CM000677.2:g.43599668A=	GRCh38
NC_000015.9:g.43891866A= , CM000677.1:g.43891866A=	GRCh37
NC_000015.8:g.41679158A=	NCBI36
NG_011636.1:g.24133T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.*4T= (STRC) MANE Select	ENSP00000401513.2:n.*4T=
ENST00000411560.1:n.142+135A= (CKMT1B)
ENST00000428650.5:c.*2365T= (STRC)	ENSP00000415991.1:n.*2365T=
ENST00000440125.5:c.*3124T= (STRC)	ENSP00000394866.1:n.*3124T=
ENST00000448437.6:n.2452T= (STRC)
ENST00000450892.6:c.*4T= (STRC)	ENSP00000401513.2:n.*4T=
ENST00000471703.5:n.3286T= (STRC)
ENST00000485556.5:n.4187T= (STRC)
ENST00000541030.5:c.*4T= (STRC)	ENSP00000440413.1:n.*4T=
NM_153700.2:c.*4T= (STRC) MANE Select	NP_714544.1:n.*4T=
XM_011521277.1:c.*4T= (STRC)	XP_011519579.1:n.*4T=
XM_011521278.1:c.*4T= (STRC)	XP_011519580.1:n.*4T=
XM_011521279.1:c.*4T= (STRC)	XP_011519581.1:n.*4T=