Canonical Allele Identifier: CA392160063

Gene: STRC CKMT1B

Linked Data

• dbSNP Id: rs2085656982
• MyVariant Identifiers: chr15:g.43892759T>A (hg19) ; chr15:g.43600561T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43600561T>A , CM000677.2:g.43600561T>A	GRCh38
NC_000015.9:g.43892759T>A , CM000677.1:g.43892759T>A	GRCh37
NC_000015.8:g.41680051T>A	NCBI36
NG_011636.1:g.23240A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000450892.7:c.4966A>T (STRC) MANE Select	ENSP00000401513.2:p.Ile1656Phe
ENST00000411560.1:n.142+1028T>A (CKMT1B)
ENST00000428650.5:c.*1999A>T (STRC)	ENSP00000415991.1:n.*1999A>T
ENST00000440125.5:c.*2758A>T (STRC)	ENSP00000394866.1:n.*2758A>T
ENST00000448437.6:n.2086A>T (STRC)
ENST00000450892.6:c.4966A>T (STRC)	ENSP00000401513.2:p.Ile1656Phe
ENST00000471703.5:n.2920A>T (STRC)
ENST00000485556.5:n.3821A>T (STRC)
ENST00000541030.5:c.2647A>T (STRC)	ENSP00000440413.1:p.Ile883Phe
NM_153700.2:c.4966A>T (STRC) MANE Select	NP_714544.1:p.Ile1656Phe
XM_011521277.1:c.5455A>T (STRC)	XP_011519579.1:p.Ile1819Phe
XM_011521278.1:c.5071A>T (STRC)	XP_011519580.1:p.Ile1691Phe
XM_011521279.1:c.5071A>T (STRC)	XP_011519581.1:p.Ile1691Phe