Canonical Allele Identifier: CA2173248293

Gene: STRC CKMT1B

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43600976A= , CM000677.2:g.43600976A=	GRCh38
NC_000015.9:g.43893174A= , CM000677.1:g.43893174A=	GRCh37
NC_000015.8:g.41680466A=	NCBI36
NG_011636.1:g.22825T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.4740T= (STRC) MANE Select	ENSP00000401513.2:p.Gly1580=
ENST00000411560.1:n.142+1443A= (CKMT1B)
ENST00000428650.5:c.*1773T= (STRC)	ENSP00000415991.1:n.*1773T=
ENST00000440125.5:c.*2532T= (STRC)	ENSP00000394866.1:n.*2532T=
ENST00000448437.6:n.1860T= (STRC)
ENST00000450892.6:c.4740T= (STRC)	ENSP00000401513.2:p.Gly1580=
ENST00000460952.1:n.319T= (STRC)
ENST00000471703.5:n.2694T= (STRC)
ENST00000485556.5:n.3595T= (STRC)
ENST00000541030.5:c.2421T= (STRC)	ENSP00000440413.1:p.Gly807=
NM_153700.2:c.4740T= (STRC) MANE Select	NP_714544.1:p.Gly1580=
XM_011521277.1:c.5229T= (STRC)	XP_011519579.1:p.Gly1743=
XM_011521278.1:c.4845T= (STRC)	XP_011519580.1:p.Gly1615=
XM_011521279.1:c.4845T= (STRC)	XP_011519581.1:p.Gly1615=