Canonical Allele Identifier: CA490144725

Gene: STRC CKMT1B

Linked Data

• MyVariant Identifiers: chr15:g.43892745A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43600547A>G , CM000677.2:g.43600547A>G	GRCh38
NC_000015.9:g.43892745A>G , CM000677.1:g.43892745A>G	GRCh37
NC_000015.8:g.41680037A>G	NCBI36
NG_011636.1:g.23254T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.4980T>C (STRC) MANE Select	ENSP00000401513.2:p.Ile1660=
ENST00000411560.1:n.142+1014A>G (CKMT1B)
ENST00000428650.5:c.*2013T>C (STRC)	ENSP00000415991.1:n.*2013T>C
ENST00000440125.5:c.*2772T>C (STRC)	ENSP00000394866.1:n.*2772T>C
ENST00000448437.6:n.2100T>C (STRC)
ENST00000450892.6:c.4980T>C (STRC)	ENSP00000401513.2:p.Ile1660=
ENST00000471703.5:n.2934T>C (STRC)
ENST00000485556.5:n.3835T>C (STRC)
ENST00000541030.5:c.2661T>C (STRC)	ENSP00000440413.1:p.Ile887=
NM_153700.2:c.4980T>C (STRC) MANE Select	NP_714544.1:p.Ile1660=
XM_011521277.1:c.5469T>C (STRC)	XP_011519579.1:p.Ile1823=
XM_011521278.1:c.5085T>C (STRC)	XP_011519580.1:p.Ile1695=
XM_011521279.1:c.5085T>C (STRC)	XP_011519581.1:p.Ile1695=