Canonical Allele Identifier: CA2173251921

Gene: STRC CKMT1B

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43604395G= , CM000677.2:g.43604395G=	GRCh38
NC_000015.9:g.43896593G= , CM000677.1:g.43896593G=	GRCh37
NC_000015.8:g.41683885G=	NCBI36
NG_011636.1:g.19406C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000450892.7:c.4184C= (STRC) MANE Select	ENSP00000401513.2:p.Thr1395=
ENST00000411560.1:n.143-389G= (CKMT1B)
ENST00000428650.5:c.*1387C= (STRC)	ENSP00000415991.1:n.*1387C=
ENST00000440125.5:c.*1976C= (STRC)	ENSP00000394866.1:n.*1976C=
ENST00000448437.6:n.1666-2844C= (STRC)
ENST00000450892.6:c.4184C= (STRC)	ENSP00000401513.2:p.Thr1395=
ENST00000471703.5:n.2138C= (STRC)
ENST00000485556.5:n.3039C= (STRC)
ENST00000541030.5:c.1865C= (STRC)	ENSP00000440413.1:p.Thr622=
NM_153700.2:c.4184C= (STRC) MANE Select	NP_714544.1:p.Thr1395=
XM_011521277.1:c.4673C= (STRC)	XP_011519579.1:p.Thr1558=
XM_011521278.1:c.4289C= (STRC)	XP_011519580.1:p.Thr1430=
XM_011521279.1:c.4289C= (STRC)	XP_011519581.1:p.Thr1430=