Canonical Allele Identifier: CA2173248053

Gene: STRC CKMT1B

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43600506T= , CM000677.2:g.43600506T=	GRCh38
NC_000015.9:g.43892704T= , CM000677.1:g.43892704T=	GRCh37
NC_000015.8:g.41679996T=	NCBI36
NG_011636.1:g.23295A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.4993+28A= (STRC) MANE Select	ENSP00000401513.2:n.4993+28A=
ENST00000411560.1:n.142+973T= (CKMT1B)
ENST00000428650.5:c.*2026+28A= (STRC)	ENSP00000415991.1:n.*2026+28A=
ENST00000440125.5:c.*2785+28A= (STRC)	ENSP00000394866.1:n.*2785+28A=
ENST00000448437.6:n.2113+28A= (STRC)
ENST00000450892.6:c.4993+28A= (STRC)	ENSP00000401513.2:n.4993+28A=
ENST00000471703.5:n.2947+28A= (STRC)
ENST00000485556.5:n.3848+28A= (STRC)
ENST00000541030.5:c.2674+28A= (STRC)	ENSP00000440413.1:n.2674+28A=
NM_153700.2:c.4993+28A= (STRC) MANE Select	NP_714544.1:n.4993+28A=
XM_011521277.1:c.5482+28A= (STRC)	XP_011519579.1:n.5482+28A=
XM_011521278.1:c.5098+28A= (STRC)	XP_011519580.1:n.5098+28A=
XM_011521279.1:c.5098+28A= (STRC)	XP_011519581.1:n.5098+28A=