Canonical Allele Identifier: CA2173248092

Gene: STRC CKMT1B

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43600596C= , CM000677.2:g.43600596C=	GRCh38
NC_000015.9:g.43892794C= , CM000677.1:g.43892794C=	GRCh37
NC_000015.8:g.41680086C=	NCBI36
NG_011636.1:g.23205G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.4931G= (STRC) MANE Select	ENSP00000401513.2:p.Gly1644=
ENST00000411560.1:n.142+1063C= (CKMT1B)
ENST00000428650.5:c.*1964G= (STRC)	ENSP00000415991.1:n.*1964G=
ENST00000440125.5:c.*2723G= (STRC)	ENSP00000394866.1:n.*2723G=
ENST00000448437.6:n.2051G= (STRC)
ENST00000450892.6:c.4931G= (STRC)	ENSP00000401513.2:p.Gly1644=
ENST00000460952.1:n.510G= (STRC)
ENST00000471703.5:n.2885G= (STRC)
ENST00000485556.5:n.3786G= (STRC)
ENST00000541030.5:c.2612G= (STRC)	ENSP00000440413.1:p.Gly871=
NM_153700.2:c.4931G= (STRC) MANE Select	NP_714544.1:p.Gly1644=
XM_011521277.1:c.5420G= (STRC)	XP_011519579.1:p.Gly1807=
XM_011521278.1:c.5036G= (STRC)	XP_011519580.1:p.Gly1679=
XM_011521279.1:c.5036G= (STRC)	XP_011519581.1:p.Gly1679=