Canonical Allele Identifier: CA2173248598

Gene: STRC CKMT1B

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43601542G= , CM000677.2:g.43601542G=	GRCh38
NC_000015.9:g.43893740G= , CM000677.1:g.43893740G=	GRCh37
NC_000015.8:g.41681032G=	NCBI36
NG_011636.1:g.22259C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.4555C= (STRC) MANE Select	ENSP00000401513.2:p.Pro1519=
ENST00000411560.1:n.142+2009G= (CKMT1B)
ENST00000428650.5:c.*1588C= (STRC)	ENSP00000415991.1:n.*1588C=
ENST00000440125.5:c.*2347C= (STRC)	ENSP00000394866.1:n.*2347C=
ENST00000448437.6:n.1675C= (STRC)
ENST00000450892.6:c.4555C= (STRC)	ENSP00000401513.2:p.Pro1519=
ENST00000460952.1:n.134C= (STRC)
ENST00000471703.5:n.2509C= (STRC)
ENST00000485556.5:n.3410C= (STRC)
ENST00000493750.1:n.351C= (STRC)
ENST00000541030.5:c.2236C= (STRC)	ENSP00000440413.1:p.Pro746=
NM_153700.2:c.4555C= (STRC) MANE Select	NP_714544.1:p.Pro1519=
XM_011521277.1:c.5044C= (STRC)	XP_011519579.1:p.Pro1682=
XM_011521278.1:c.4660C= (STRC)	XP_011519580.1:p.Pro1554=
XM_011521279.1:c.4660C= (STRC)	XP_011519581.1:p.Pro1554=