Canonical Allele Identifier: CA490148478

Gene: STRC CKMT1B

Linked Data

• MyVariant Identifiers: chr15:g.43896589C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43604391C>G , CM000677.2:g.43604391C>G	GRCh38
NC_000015.9:g.43896589C>G , CM000677.1:g.43896589C>G	GRCh37
NC_000015.8:g.41683881C>G	NCBI36
NG_011636.1:g.19410G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.4188G>C (STRC) MANE Select	ENSP00000401513.2:p.Leu1396=
ENST00000411560.1:n.143-393C>G (CKMT1B)
ENST00000428650.5:c.*1391G>C (STRC)	ENSP00000415991.1:n.*1391G>C
ENST00000440125.5:c.*1980G>C (STRC)	ENSP00000394866.1:n.*1980G>C
ENST00000448437.6:n.1666-2840G>C (STRC)
ENST00000450892.6:c.4188G>C (STRC)	ENSP00000401513.2:p.Leu1396=
ENST00000471703.5:n.2142G>C (STRC)
ENST00000485556.5:n.3043G>C (STRC)
ENST00000541030.5:c.1869G>C (STRC)	ENSP00000440413.1:p.Leu623=
NM_153700.2:c.4188G>C (STRC) MANE Select	NP_714544.1:p.Leu1396=
XM_011521277.1:c.4677G>C (STRC)	XP_011519579.1:p.Leu1559=
XM_011521278.1:c.4293G>C (STRC)	XP_011519580.1:p.Leu1431=
XM_011521279.1:c.4293G>C (STRC)	XP_011519581.1:p.Leu1431=