Canonical Allele Identifier: CA2173248248

Gene: STRC CKMT1B

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43600884C= , CM000677.2:g.43600884C=	GRCh38
NC_000015.9:g.43893082C= , CM000677.1:g.43893082C=	GRCh37
NC_000015.8:g.41680374C=	NCBI36
NG_011636.1:g.22917G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000450892.7:c.4832G= (STRC) MANE Select	ENSP00000401513.2:p.Ser1611=
ENST00000411560.1:n.142+1351C= (CKMT1B)
ENST00000428650.5:c.*1865G= (STRC)	ENSP00000415991.1:n.*1865G=
ENST00000440125.5:c.*2624G= (STRC)	ENSP00000394866.1:n.*2624G=
ENST00000448437.6:n.1952G= (STRC)
ENST00000450892.6:c.4832G= (STRC)	ENSP00000401513.2:p.Ser1611=
ENST00000460952.1:n.411G= (STRC)
ENST00000471703.5:n.2786G= (STRC)
ENST00000485556.5:n.3687G= (STRC)
ENST00000541030.5:c.2513G= (STRC)	ENSP00000440413.1:p.Ser838=
NM_153700.2:c.4832G= (STRC) MANE Select	NP_714544.1:p.Ser1611=
XM_011521277.1:c.5321G= (STRC)	XP_011519579.1:p.Ser1774=
XM_011521278.1:c.4937G= (STRC)	XP_011519580.1:p.Ser1646=
XM_011521279.1:c.4937G= (STRC)	XP_011519581.1:p.Ser1646=