Canonical Allele Identifier: CA490144176

Gene: STRC CKMT1B

Linked Data

• MyVariant Identifiers: chr15:g.43891894G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43599696G>A , CM000677.2:g.43599696G>A	GRCh38
NC_000015.9:g.43891894G>A , CM000677.1:g.43891894G>A	GRCh37
NC_000015.8:g.41679186G>A	NCBI36
NG_011636.1:g.24105C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.5304C>T (STRC) MANE Select	ENSP00000401513.2:p.Ile1768=
ENST00000411560.1:n.142+163G>A (CKMT1B)
ENST00000428650.5:c.*2337C>T (STRC)	ENSP00000415991.1:n.*2337C>T
ENST00000440125.5:c.*3096C>T (STRC)	ENSP00000394866.1:n.*3096C>T
ENST00000448437.6:n.2424C>T (STRC)
ENST00000450892.6:c.5304C>T (STRC)	ENSP00000401513.2:p.Ile1768=
ENST00000471703.5:n.3258C>T (STRC)
ENST00000485556.5:n.4159C>T (STRC)
ENST00000541030.5:c.2985C>T (STRC)	ENSP00000440413.1:p.Ile995=
NM_153700.2:c.5304C>T (STRC) MANE Select	NP_714544.1:p.Ile1768=
XM_011521277.1:c.5793C>T (STRC)	XP_011519579.1:p.Ile1931=
XM_011521278.1:c.5409C>T (STRC)	XP_011519580.1:p.Ile1803=
XM_011521279.1:c.5409C>T (STRC)	XP_011519581.1:p.Ile1803=