Canonical Allele Identifier: CA2173247744

Gene: STRC CKMT1B

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43599609C= , CM000677.2:g.43599609C=	GRCh38
NC_000015.9:g.43891807C= , CM000677.1:g.43891807C=	GRCh37
NC_000015.8:g.41679099C=	NCBI36
NG_011636.1:g.24192G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.*63G= (STRC) MANE Select	ENSP00000401513.2:n.*63G=
ENST00000411560.1:n.142+76C= (CKMT1B)
ENST00000448437.6:n.2511G= (STRC)
ENST00000450892.6:c.*63G= (STRC)	ENSP00000401513.2:n.*63G=
ENST00000471703.5:n.3345G= (STRC)
ENST00000485556.5:n.4246G= (STRC)
ENST00000541030.5:c.*63G= (STRC)	ENSP00000440413.1:n.*63G=
NM_153700.2:c.*63G= (STRC) MANE Select	NP_714544.1:n.*63G=
XM_011521277.1:c.*63G= (STRC)	XP_011519579.1:n.*63G=
XM_011521278.1:c.*63G= (STRC)	XP_011519580.1:n.*63G=
XM_011521279.1:c.*63G= (STRC)	XP_011519581.1:n.*63G=