Canonical Allele Identifier: CA392157432

Gene: STRC CKMT1B

Linked Data

• MyVariant Identifiers: chr15:g.43891889A>G (hg19) ; chr15:g.43599691A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43599691A>G , CM000677.2:g.43599691A>G	GRCh38
NC_000015.9:g.43891889A>G , CM000677.1:g.43891889A>G	GRCh37
NC_000015.8:g.41679181A>G	NCBI36
NG_011636.1:g.24110T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.5309T>C (STRC) MANE Select	ENSP00000401513.2:p.Phe1770Ser
ENST00000411560.1:n.142+158A>G (CKMT1B)
ENST00000428650.5:c.*2342T>C (STRC)	ENSP00000415991.1:n.*2342T>C
ENST00000440125.5:c.*3101T>C (STRC)	ENSP00000394866.1:n.*3101T>C
ENST00000448437.6:n.2429T>C (STRC)
ENST00000450892.6:c.5309T>C (STRC)	ENSP00000401513.2:p.Phe1770Ser
ENST00000471703.5:n.3263T>C (STRC)
ENST00000485556.5:n.4164T>C (STRC)
ENST00000541030.5:c.2990T>C (STRC)	ENSP00000440413.1:p.Phe997Ser
NM_153700.2:c.5309T>C (STRC) MANE Select	NP_714544.1:p.Phe1770Ser
XM_011521277.1:c.5798T>C (STRC)	XP_011519579.1:p.Phe1933Ser
XM_011521278.1:c.5414T>C (STRC)	XP_011519580.1:p.Phe1805Ser
XM_011521279.1:c.5414T>C (STRC)	XP_011519581.1:p.Phe1805Ser