Canonical Allele Identifier: CA2173248044

Gene: STRC CKMT1B

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43600490T= , CM000677.2:g.43600490T=	GRCh38
NC_000015.9:g.43892688T= , CM000677.1:g.43892688T=	GRCh37
NC_000015.8:g.41679980T=	NCBI36
NG_011636.1:g.23311A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.4993+44A= (STRC) MANE Select	ENSP00000401513.2:n.4993+44A=
ENST00000411560.1:n.142+957T= (CKMT1B)
ENST00000428650.5:c.*2026+44A= (STRC)	ENSP00000415991.1:n.*2026+44A=
ENST00000440125.5:c.*2785+44A= (STRC)	ENSP00000394866.1:n.*2785+44A=
ENST00000448437.6:n.2113+44A= (STRC)
ENST00000450892.6:c.4993+44A= (STRC)	ENSP00000401513.2:n.4993+44A=
ENST00000471703.5:n.2947+44A= (STRC)
ENST00000485556.5:n.3848+44A= (STRC)
ENST00000541030.5:c.2674+44A= (STRC)	ENSP00000440413.1:n.2674+44A=
NM_153700.2:c.4993+44A= (STRC) MANE Select	NP_714544.1:n.4993+44A=
XM_011521277.1:c.5482+44A= (STRC)	XP_011519579.1:n.5482+44A=
XM_011521278.1:c.5098+44A= (STRC)	XP_011519580.1:n.5098+44A=
XM_011521279.1:c.5098+44A= (STRC)	XP_011519581.1:n.5098+44A=