Canonical Allele Identifier: CA490144732

Gene: STRC CKMT1B

Linked Data

• MyVariant Identifiers: chr15:g.43892748T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43600550T>C , CM000677.2:g.43600550T>C	GRCh38
NC_000015.9:g.43892748T>C , CM000677.1:g.43892748T>C	GRCh37
NC_000015.8:g.41680040T>C	NCBI36
NG_011636.1:g.23251A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000450892.7:c.4977A>G (STRC) MANE Select	ENSP00000401513.2:p.Glu1659=
ENST00000411560.1:n.142+1017T>C (CKMT1B)
ENST00000428650.5:c.*2010A>G (STRC)	ENSP00000415991.1:n.*2010A>G
ENST00000440125.5:c.*2769A>G (STRC)	ENSP00000394866.1:n.*2769A>G
ENST00000448437.6:n.2097A>G (STRC)
ENST00000450892.6:c.4977A>G (STRC)	ENSP00000401513.2:p.Glu1659=
ENST00000471703.5:n.2931A>G (STRC)
ENST00000485556.5:n.3832A>G (STRC)
ENST00000541030.5:c.2658A>G (STRC)	ENSP00000440413.1:p.Glu886=
NM_153700.2:c.4977A>G (STRC) MANE Select	NP_714544.1:p.Glu1659=
XM_011521277.1:c.5466A>G (STRC)	XP_011519579.1:p.Glu1822=
XM_011521278.1:c.5082A>G (STRC)	XP_011519580.1:p.Glu1694=
XM_011521279.1:c.5082A>G (STRC)	XP_011519581.1:p.Glu1694=