Canonical Allele Identifier: CA2173251853

Gene: STRC CKMT1B

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43604305C= , CM000677.2:g.43604305C=	GRCh38
NC_000015.9:g.43896503C= , CM000677.1:g.43896503C=	GRCh37
NC_000015.8:g.41683795C=	NCBI36
NG_011636.1:g.19496G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.4218+56G= (STRC) MANE Select	ENSP00000401513.2:n.4218+56G=
ENST00000411560.1:n.143-479C= (CKMT1B)
ENST00000428650.5:c.*1421+56G= (STRC)	ENSP00000415991.1:n.*1421+56G=
ENST00000440125.5:c.*2010+56G= (STRC)	ENSP00000394866.1:n.*2010+56G=
ENST00000448437.6:n.1666-2754G= (STRC)
ENST00000450892.6:c.4218+56G= (STRC)	ENSP00000401513.2:n.4218+56G=
ENST00000471703.5:n.2172+56G= (STRC)
ENST00000485556.5:n.3073+56G= (STRC)
ENST00000541030.5:c.1899+56G= (STRC)	ENSP00000440413.1:n.1899+56G=
NM_153700.2:c.4218+56G= (STRC) MANE Select	NP_714544.1:n.4218+56G=
XM_011521277.1:c.4707+56G= (STRC)	XP_011519579.1:n.4707+56G=
XM_011521278.1:c.4323+56G= (STRC)	XP_011519580.1:n.4323+56G=
XM_011521279.1:c.4323+56G= (STRC)	XP_011519581.1:n.4323+56G=