Canonical Allele Identifier: CA490144226

Gene: STRC CKMT1B

Linked Data

• MyVariant Identifiers: chr15:g.43891957A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43599759A>G , CM000677.2:g.43599759A>G	GRCh38
NC_000015.9:g.43891957A>G , CM000677.1:g.43891957A>G	GRCh37
NC_000015.8:g.41679249A>G	NCBI36
NG_011636.1:g.24042T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.5241T>C (STRC) MANE Select	ENSP00000401513.2:p.Gly1747=
ENST00000411560.1:n.142+226A>G (CKMT1B)
ENST00000428650.5:c.*2274T>C (STRC)	ENSP00000415991.1:n.*2274T>C
ENST00000440125.5:c.*3033T>C (STRC)	ENSP00000394866.1:n.*3033T>C
ENST00000448437.6:n.2361T>C (STRC)
ENST00000450892.6:c.5241T>C (STRC)	ENSP00000401513.2:p.Gly1747=
ENST00000471703.5:n.3195T>C (STRC)
ENST00000485556.5:n.4096T>C (STRC)
ENST00000541030.5:c.2922T>C (STRC)	ENSP00000440413.1:p.Gly974=
NM_153700.2:c.5241T>C (STRC) MANE Select	NP_714544.1:p.Gly1747=
XM_011521277.1:c.5730T>C (STRC)	XP_011519579.1:p.Gly1910=
XM_011521278.1:c.5346T>C (STRC)	XP_011519580.1:p.Gly1782=
XM_011521279.1:c.5346T>C (STRC)	XP_011519581.1:p.Gly1782=