Canonical Allele Identifier: CA2173247792

Gene: STRC CKMT1B

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43599787T= , CM000677.2:g.43599787T=	GRCh38
NC_000015.9:g.43891985T= , CM000677.1:g.43891985T=	GRCh37
NC_000015.8:g.41679277T=	NCBI36
NG_011636.1:g.24014A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.5240-27A= (STRC) MANE Select	ENSP00000401513.2:n.5240-27A=
ENST00000411560.1:n.142+254T= (CKMT1B)
ENST00000428650.5:c.*2273-27A= (STRC)	ENSP00000415991.1:n.*2273-27A=
ENST00000440125.5:c.*3032-27A= (STRC)	ENSP00000394866.1:n.*3032-27A=
ENST00000448437.6:n.2360-27A= (STRC)
ENST00000450892.6:c.5240-27A= (STRC)	ENSP00000401513.2:n.5240-27A=
ENST00000471703.5:n.3194-27A= (STRC)
ENST00000485556.5:n.4095-27A= (STRC)
ENST00000541030.5:c.2921-27A= (STRC)	ENSP00000440413.1:n.2921-27A=
NM_153700.2:c.5240-27A= (STRC) MANE Select	NP_714544.1:n.5240-27A=
XM_011521277.1:c.5729-27A= (STRC)	XP_011519579.1:n.5729-27A=
XM_011521278.1:c.5345-27A= (STRC)	XP_011519580.1:n.5345-27A=
XM_011521279.1:c.5345-27A= (STRC)	XP_011519581.1:n.5345-27A=