Canonical Allele Identifier: CA392162166

Gene: STRC CKMT1B

Linked Data

• MyVariant Identifiers: chr15:g.43892848A>G (hg19) ; chr15:g.43600650A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43600650A>G , CM000677.2:g.43600650A>G	GRCh38
NC_000015.9:g.43892848A>G , CM000677.1:g.43892848A>G	GRCh37
NC_000015.8:g.41680140A>G	NCBI36
NG_011636.1:g.23151T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000450892.7:c.4877T>C (STRC) MANE Select	ENSP00000401513.2:p.Leu1626Pro
ENST00000411560.1:n.142+1117A>G (CKMT1B)
ENST00000428650.5:c.*1910T>C (STRC)	ENSP00000415991.1:n.*1910T>C
ENST00000440125.5:c.*2669T>C (STRC)	ENSP00000394866.1:n.*2669T>C
ENST00000448437.6:n.1997T>C (STRC)
ENST00000450892.6:c.4877T>C (STRC)	ENSP00000401513.2:p.Leu1626Pro
ENST00000460952.1:n.456T>C (STRC)
ENST00000471703.5:n.2831T>C (STRC)
ENST00000485556.5:n.3732T>C (STRC)
ENST00000541030.5:c.2558T>C (STRC)	ENSP00000440413.1:p.Leu853Pro
NM_153700.2:c.4877T>C (STRC) MANE Select	NP_714544.1:p.Leu1626Pro
XM_011521277.1:c.5366T>C (STRC)	XP_011519579.1:p.Leu1789Pro
XM_011521278.1:c.4982T>C (STRC)	XP_011519580.1:p.Leu1661Pro
XM_011521279.1:c.4982T>C (STRC)	XP_011519581.1:p.Leu1661Pro