Canonical Allele Identifier: CA490145363

Gene: STRC CKMT1B

Linked Data

• MyVariant Identifiers: chr15:g.43893648C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43601450C>A , CM000677.2:g.43601450C>A	GRCh38
NC_000015.9:g.43893648C>A , CM000677.1:g.43893648C>A	GRCh37
NC_000015.8:g.41680940C>A	NCBI36
NG_011636.1:g.22351G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.4647G>T (STRC) MANE Select	ENSP00000401513.2:p.Val1549=
ENST00000411560.1:n.142+1917C>A (CKMT1B)
ENST00000428650.5:c.*1680G>T (STRC)	ENSP00000415991.1:n.*1680G>T
ENST00000440125.5:c.*2439G>T (STRC)	ENSP00000394866.1:n.*2439G>T
ENST00000448437.6:n.1767G>T (STRC)
ENST00000450892.6:c.4647G>T (STRC)	ENSP00000401513.2:p.Val1549=
ENST00000460952.1:n.226G>T (STRC)
ENST00000471703.5:n.2601G>T (STRC)
ENST00000485556.5:n.3502G>T (STRC)
ENST00000493750.1:n.443G>T (STRC)
ENST00000541030.5:c.2328G>T (STRC)	ENSP00000440413.1:p.Val776=
NM_153700.2:c.4647G>T (STRC) MANE Select	NP_714544.1:p.Val1549=
XM_011521277.1:c.5136G>T (STRC)	XP_011519579.1:p.Val1712=
XM_011521278.1:c.4752G>T (STRC)	XP_011519580.1:p.Val1584=
XM_011521279.1:c.4752G>T (STRC)	XP_011519581.1:p.Val1584=