Canonical Allele Identifier: CA490144846

Gene: STRC CKMT1B

Linked Data

• gnomAD v4: 15-43600601-C-A
• MyVariant Identifiers: chr15:g.43892799C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43600601C>A , CM000677.2:g.43600601C>A	GRCh38
NC_000015.9:g.43892799C>A , CM000677.1:g.43892799C>A	GRCh37
NC_000015.8:g.41680091C>A	NCBI36
NG_011636.1:g.23200G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.4926G>T (STRC) MANE Select	ENSP00000401513.2:p.Leu1642=
ENST00000411560.1:n.142+1068C>A (CKMT1B)
ENST00000428650.5:c.*1959G>T (STRC)	ENSP00000415991.1:n.*1959G>T
ENST00000440125.5:c.*2718G>T (STRC)	ENSP00000394866.1:n.*2718G>T
ENST00000448437.6:n.2046G>T (STRC)
ENST00000450892.6:c.4926G>T (STRC)	ENSP00000401513.2:p.Leu1642=
ENST00000460952.1:n.505G>T (STRC)
ENST00000471703.5:n.2880G>T (STRC)
ENST00000485556.5:n.3781G>T (STRC)
ENST00000541030.5:c.2607G>T (STRC)	ENSP00000440413.1:p.Leu869=
NM_153700.2:c.4926G>T (STRC) MANE Select	NP_714544.1:p.Leu1642=
XM_011521277.1:c.5415G>T (STRC)	XP_011519579.1:p.Leu1805=
XM_011521278.1:c.5031G>T (STRC)	XP_011519580.1:p.Leu1677=
XM_011521279.1:c.5031G>T (STRC)	XP_011519581.1:p.Leu1677=