Canonical Allele Identifier: CA490148419

Gene: STRC CKMT1B

Linked Data

• MyVariant Identifiers: chr15:g.43896574A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43604376A>G , CM000677.2:g.43604376A>G	GRCh38
NC_000015.9:g.43896574A>G , CM000677.1:g.43896574A>G	GRCh37
NC_000015.8:g.41683866A>G	NCBI36
NG_011636.1:g.19425T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.4203T>C (STRC) MANE Select	ENSP00000401513.2:p.Ile1401=
ENST00000411560.1:n.143-408A>G (CKMT1B)
ENST00000428650.5:c.*1406T>C (STRC)	ENSP00000415991.1:n.*1406T>C
ENST00000440125.5:c.*1995T>C (STRC)	ENSP00000394866.1:n.*1995T>C
ENST00000448437.6:n.1666-2825T>C (STRC)
ENST00000450892.6:c.4203T>C (STRC)	ENSP00000401513.2:p.Ile1401=
ENST00000471703.5:n.2157T>C (STRC)
ENST00000485556.5:n.3058T>C (STRC)
ENST00000541030.5:c.1884T>C (STRC)	ENSP00000440413.1:p.Ile628=
NM_153700.2:c.4203T>C (STRC) MANE Select	NP_714544.1:p.Ile1401=
XM_011521277.1:c.4692T>C (STRC)	XP_011519579.1:p.Ile1564=
XM_011521278.1:c.4308T>C (STRC)	XP_011519580.1:p.Ile1436=
XM_011521279.1:c.4308T>C (STRC)	XP_011519581.1:p.Ile1436=