Canonical Allele Identifier: CA2173248108

Gene: STRC CKMT1B

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43600624C= , CM000677.2:g.43600624C=	GRCh38
NC_000015.9:g.43892822C= , CM000677.1:g.43892822C=	GRCh37
NC_000015.8:g.41680114C=	NCBI36
NG_011636.1:g.23177G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.4903G= (STRC) MANE Select	ENSP00000401513.2:p.Val1635=
ENST00000411560.1:n.142+1091C= (CKMT1B)
ENST00000428650.5:c.*1936G= (STRC)	ENSP00000415991.1:n.*1936G=
ENST00000440125.5:c.*2695G= (STRC)	ENSP00000394866.1:n.*2695G=
ENST00000448437.6:n.2023G= (STRC)
ENST00000450892.6:c.4903G= (STRC)	ENSP00000401513.2:p.Val1635=
ENST00000460952.1:n.482G= (STRC)
ENST00000471703.5:n.2857G= (STRC)
ENST00000485556.5:n.3758G= (STRC)
ENST00000541030.5:c.2584G= (STRC)	ENSP00000440413.1:p.Val862=
NM_153700.2:c.4903G= (STRC) MANE Select	NP_714544.1:p.Val1635=
XM_011521277.1:c.5392G= (STRC)	XP_011519579.1:p.Val1798=
XM_011521278.1:c.5008G= (STRC)	XP_011519580.1:p.Val1670=
XM_011521279.1:c.5008G= (STRC)	XP_011519581.1:p.Val1670=