Canonical Allele Identifier: CA2173252276

Gene: STRC CKMT1B

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43604726G= , CM000677.2:g.43604726G=	GRCh38
NC_000015.9:g.43896924G= , CM000677.1:g.43896924G=	GRCh37
NC_000015.8:g.41684216G=	NCBI36
NG_011636.1:g.19075C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.4051C= (STRC) MANE Select	ENSP00000401513.2:p.Gln1351=
ENST00000411560.1:n.143-58G= (CKMT1B)
ENST00000428650.5:c.*1254C= (STRC)	ENSP00000415991.1:n.*1254C=
ENST00000440125.5:c.*1843C= (STRC)	ENSP00000394866.1:n.*1843C=
ENST00000448437.6:n.1665+3137C= (STRC)
ENST00000450892.6:c.4051C= (STRC)	ENSP00000401513.2:p.Gln1351=
ENST00000455136.5:c.1082C= (STRC)
ENST00000471703.5:n.2005C= (STRC)
ENST00000485556.5:n.2906C= (STRC)
ENST00000541030.5:c.1732C= (STRC)	ENSP00000440413.1:p.Gln578=
NM_153700.2:c.4051C= (STRC) MANE Select	NP_714544.1:p.Gln1351=
XM_011521277.1:c.4540C= (STRC)	XP_011519579.1:p.Gln1514=
XM_011521278.1:c.4156C= (STRC)	XP_011519580.1:p.Gln1386=
XM_011521279.1:c.4156C= (STRC)	XP_011519581.1:p.Gln1386=