Canonical Allele Identifier: CA490144198

Gene: STRC CKMT1B

Linked Data

• MyVariant Identifiers: chr15:g.43891918A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43599720A>T , CM000677.2:g.43599720A>T	GRCh38
NC_000015.9:g.43891918A>T , CM000677.1:g.43891918A>T	GRCh37
NC_000015.8:g.41679210A>T	NCBI36
NG_011636.1:g.24081T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.5280T>A (STRC) MANE Select	ENSP00000401513.2:p.Pro1760=
ENST00000411560.1:n.142+187A>T (CKMT1B)
ENST00000428650.5:c.*2313T>A (STRC)	ENSP00000415991.1:n.*2313T>A
ENST00000440125.5:c.*3072T>A (STRC)	ENSP00000394866.1:n.*3072T>A
ENST00000448437.6:n.2400T>A (STRC)
ENST00000450892.6:c.5280T>A (STRC)	ENSP00000401513.2:p.Pro1760=
ENST00000471703.5:n.3234T>A (STRC)
ENST00000485556.5:n.4135T>A (STRC)
ENST00000541030.5:c.2961T>A (STRC)	ENSP00000440413.1:p.Pro987=
NM_153700.2:c.5280T>A (STRC) MANE Select	NP_714544.1:p.Pro1760=
XM_011521277.1:c.5769T>A (STRC)	XP_011519579.1:p.Pro1923=
XM_011521278.1:c.5385T>A (STRC)	XP_011519580.1:p.Pro1795=
XM_011521279.1:c.5385T>A (STRC)	XP_011519581.1:p.Pro1795=