Canonical Allele Identifier: CA490144827

Gene: STRC CKMT1B

Linked Data

• MyVariant Identifiers: chr15:g.43892790C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43600592C>T , CM000677.2:g.43600592C>T	GRCh38
NC_000015.9:g.43892790C>T , CM000677.1:g.43892790C>T	GRCh37
NC_000015.8:g.41680082C>T	NCBI36
NG_011636.1:g.23209G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.4935G>A (STRC) MANE Select	ENSP00000401513.2:p.Gly1645=
ENST00000411560.1:n.142+1059C>T (CKMT1B)
ENST00000428650.5:c.*1968G>A (STRC)	ENSP00000415991.1:n.*1968G>A
ENST00000440125.5:c.*2727G>A (STRC)	ENSP00000394866.1:n.*2727G>A
ENST00000448437.6:n.2055G>A (STRC)
ENST00000450892.6:c.4935G>A (STRC)	ENSP00000401513.2:p.Gly1645=
ENST00000460952.1:n.514G>A (STRC)
ENST00000471703.5:n.2889G>A (STRC)
ENST00000485556.5:n.3790G>A (STRC)
ENST00000541030.5:c.2616G>A (STRC)	ENSP00000440413.1:p.Gly872=
NM_153700.2:c.4935G>A (STRC) MANE Select	NP_714544.1:p.Gly1645=
XM_011521277.1:c.5424G>A (STRC)	XP_011519579.1:p.Gly1808=
XM_011521278.1:c.5040G>A (STRC)	XP_011519580.1:p.Gly1680=
XM_011521279.1:c.5040G>A (STRC)	XP_011519581.1:p.Gly1680=