Canonical Allele Identifier: CA490144996

Gene: STRC CKMT1B

Linked Data

• MyVariant Identifiers: chr15:g.43892859G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43600661G>T , CM000677.2:g.43600661G>T	GRCh38
NC_000015.9:g.43892859G>T , CM000677.1:g.43892859G>T	GRCh37
NC_000015.8:g.41680151G>T	NCBI36
NG_011636.1:g.23140C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.4866C>A (STRC) MANE Select	ENSP00000401513.2:p.Gly1622=
ENST00000411560.1:n.142+1128G>T (CKMT1B)
ENST00000428650.5:c.*1899C>A (STRC)	ENSP00000415991.1:n.*1899C>A
ENST00000440125.5:c.*2658C>A (STRC)	ENSP00000394866.1:n.*2658C>A
ENST00000448437.6:n.1986C>A (STRC)
ENST00000450892.6:c.4866C>A (STRC)	ENSP00000401513.2:p.Gly1622=
ENST00000460952.1:n.445C>A (STRC)
ENST00000471703.5:n.2820C>A (STRC)
ENST00000485556.5:n.3721C>A (STRC)
ENST00000541030.5:c.2547C>A (STRC)	ENSP00000440413.1:p.Gly849=
NM_153700.2:c.4866C>A (STRC) MANE Select	NP_714544.1:p.Gly1622=
XM_011521277.1:c.5355C>A (STRC)	XP_011519579.1:p.Gly1785=
XM_011521278.1:c.4971C>A (STRC)	XP_011519580.1:p.Gly1657=
XM_011521279.1:c.4971C>A (STRC)	XP_011519581.1:p.Gly1657=