Canonical Allele Identifier: CA490144231

Gene: STRC CKMT1B

Linked Data

• MyVariant Identifiers: chr15:g.43892168T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43599970T>G , CM000677.2:g.43599970T>G	GRCh38
NC_000015.9:g.43892168T>G , CM000677.1:g.43892168T>G	GRCh37
NC_000015.8:g.41679460T>G	NCBI36
NG_011636.1:g.23831A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.5229A>C (STRC) MANE Select	ENSP00000401513.2:p.Pro1743=
ENST00000411560.1:n.142+437T>G (CKMT1B)
ENST00000428650.5:c.*2262A>C (STRC)	ENSP00000415991.1:n.*2262A>C
ENST00000440125.5:c.*3021A>C (STRC)	ENSP00000394866.1:n.*3021A>C
ENST00000448437.6:n.2349A>C (STRC)
ENST00000450892.6:c.5229A>C (STRC)	ENSP00000401513.2:p.Pro1743=
ENST00000471703.5:n.3183A>C (STRC)
ENST00000485556.5:n.4084A>C (STRC)
ENST00000541030.5:c.2910A>C (STRC)	ENSP00000440413.1:p.Pro970=
NM_153700.2:c.5229A>C (STRC) MANE Select	NP_714544.1:p.Pro1743=
XM_011521277.1:c.5718A>C (STRC)	XP_011519579.1:p.Pro1906=
XM_011521278.1:c.5334A>C (STRC)	XP_011519580.1:p.Pro1778=
XM_011521279.1:c.5334A>C (STRC)	XP_011519581.1:p.Pro1778=