Canonical Allele Identifier: CA490144159

Gene: STRC CKMT1B

Linked Data

• MyVariant Identifiers: chr15:g.43891873T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43599675T>A , CM000677.2:g.43599675T>A	GRCh38
NC_000015.9:g.43891873T>A , CM000677.1:g.43891873T>A	GRCh37
NC_000015.8:g.41679165T>A	NCBI36
NG_011636.1:g.24126A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.5325A>T (STRC) MANE Select	ENSP00000401513.2:p.Leu1775=
ENST00000411560.1:n.142+142T>A (CKMT1B)
ENST00000428650.5:c.*2358A>T (STRC)	ENSP00000415991.1:n.*2358A>T
ENST00000440125.5:c.*3117A>T (STRC)	ENSP00000394866.1:n.*3117A>T
ENST00000448437.6:n.2445A>T (STRC)
ENST00000450892.6:c.5325A>T (STRC)	ENSP00000401513.2:p.Leu1775=
ENST00000471703.5:n.3279A>T (STRC)
ENST00000485556.5:n.4180A>T (STRC)
ENST00000541030.5:c.3006A>T (STRC)	ENSP00000440413.1:p.Leu1002=
NM_153700.2:c.5325A>T (STRC) MANE Select	NP_714544.1:p.Leu1775=
XM_011521277.1:c.5814A>T (STRC)	XP_011519579.1:p.Leu1938=
XM_011521278.1:c.5430A>T (STRC)	XP_011519580.1:p.Leu1810=
XM_011521279.1:c.5430A>T (STRC)	XP_011519581.1:p.Leu1810=