Canonical Allele Identifier: CA490148468

Gene: STRC CKMT1B

Linked Data

• MyVariant Identifiers: chr15:g.43896586A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43604388A>T , CM000677.2:g.43604388A>T	GRCh38
NC_000015.9:g.43896586A>T , CM000677.1:g.43896586A>T	GRCh37
NC_000015.8:g.41683878A>T	NCBI36
NG_011636.1:g.19413T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.4191T>A (STRC) MANE Select	ENSP00000401513.2:p.Ser1397=
ENST00000411560.1:n.143-396A>T (CKMT1B)
ENST00000428650.5:c.*1394T>A (STRC)	ENSP00000415991.1:n.*1394T>A
ENST00000440125.5:c.*1983T>A (STRC)	ENSP00000394866.1:n.*1983T>A
ENST00000448437.6:n.1666-2837T>A (STRC)
ENST00000450892.6:c.4191T>A (STRC)	ENSP00000401513.2:p.Ser1397=
ENST00000471703.5:n.2145T>A (STRC)
ENST00000485556.5:n.3046T>A (STRC)
ENST00000541030.5:c.1872T>A (STRC)	ENSP00000440413.1:p.Ser624=
NM_153700.2:c.4191T>A (STRC) MANE Select	NP_714544.1:p.Ser1397=
XM_011521277.1:c.4680T>A (STRC)	XP_011519579.1:p.Ser1560=
XM_011521278.1:c.4296T>A (STRC)	XP_011519580.1:p.Ser1432=
XM_011521279.1:c.4296T>A (STRC)	XP_011519581.1:p.Ser1432=