Canonical Allele Identifier: CA490145455

Gene: STRC CKMT1B

Linked Data

• MyVariant Identifiers: chr15:g.43893720A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43601522A>G , CM000677.2:g.43601522A>G	GRCh38
NC_000015.9:g.43893720A>G , CM000677.1:g.43893720A>G	GRCh37
NC_000015.8:g.41681012A>G	NCBI36
NG_011636.1:g.22279T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.4575T>C (STRC) MANE Select	ENSP00000401513.2:p.Pro1525=
ENST00000411560.1:n.142+1989A>G (CKMT1B)
ENST00000428650.5:c.*1608T>C (STRC)	ENSP00000415991.1:n.*1608T>C
ENST00000440125.5:c.*2367T>C (STRC)	ENSP00000394866.1:n.*2367T>C
ENST00000448437.6:n.1695T>C (STRC)
ENST00000450892.6:c.4575T>C (STRC)	ENSP00000401513.2:p.Pro1525=
ENST00000460952.1:n.154T>C (STRC)
ENST00000471703.5:n.2529T>C (STRC)
ENST00000485556.5:n.3430T>C (STRC)
ENST00000493750.1:n.371T>C (STRC)
ENST00000541030.5:c.2256T>C (STRC)	ENSP00000440413.1:p.Pro752=
NM_153700.2:c.4575T>C (STRC) MANE Select	NP_714544.1:p.Pro1525=
XM_011521277.1:c.5064T>C (STRC)	XP_011519579.1:p.Pro1688=
XM_011521278.1:c.4680T>C (STRC)	XP_011519580.1:p.Pro1560=
XM_011521279.1:c.4680T>C (STRC)	XP_011519581.1:p.Pro1560=