Canonical Allele Identifier: CA490148486

Gene: STRC CKMT1B

Linked Data

• MyVariant Identifiers: chr15:g.43896592A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43604394A>G , CM000677.2:g.43604394A>G	GRCh38
NC_000015.9:g.43896592A>G , CM000677.1:g.43896592A>G	GRCh37
NC_000015.8:g.41683884A>G	NCBI36
NG_011636.1:g.19407T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.4185T>C (STRC) MANE Select	ENSP00000401513.2:p.Thr1395=
ENST00000411560.1:n.143-390A>G (CKMT1B)
ENST00000428650.5:c.*1388T>C (STRC)	ENSP00000415991.1:n.*1388T>C
ENST00000440125.5:c.*1977T>C (STRC)	ENSP00000394866.1:n.*1977T>C
ENST00000448437.6:n.1666-2843T>C (STRC)
ENST00000450892.6:c.4185T>C (STRC)	ENSP00000401513.2:p.Thr1395=
ENST00000471703.5:n.2139T>C (STRC)
ENST00000485556.5:n.3040T>C (STRC)
ENST00000541030.5:c.1866T>C (STRC)	ENSP00000440413.1:p.Thr622=
NM_153700.2:c.4185T>C (STRC) MANE Select	NP_714544.1:p.Thr1395=
XM_011521277.1:c.4674T>C (STRC)	XP_011519579.1:p.Thr1558=
XM_011521278.1:c.4290T>C (STRC)	XP_011519580.1:p.Thr1430=
XM_011521279.1:c.4290T>C (STRC)	XP_011519581.1:p.Thr1430=