Canonical Allele Identifier: CA392163716

Gene: STRC CKMT1B

Linked Data

• dbSNP Id: rs1201686797
• gnomAD v3: 15-43601458-T-C
• gnomAD v4: 15-43601458-T-C
• MyVariant Identifiers: chr15:g.43893656T>C (hg19) ; chr15:g.43601458T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43601458T>C , CM000677.2:g.43601458T>C	GRCh38
NC_000015.9:g.43893656T>C , CM000677.1:g.43893656T>C	GRCh37
NC_000015.8:g.41680948T>C	NCBI36
NG_011636.1:g.22343A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.4639A>G (STRC) MANE Select	ENSP00000401513.2:p.Ile1547Val
ENST00000411560.1:n.142+1925T>C (CKMT1B)
ENST00000428650.5:c.*1672A>G (STRC)	ENSP00000415991.1:n.*1672A>G
ENST00000440125.5:c.*2431A>G (STRC)	ENSP00000394866.1:n.*2431A>G
ENST00000448437.6:n.1759A>G (STRC)
ENST00000450892.6:c.4639A>G (STRC)	ENSP00000401513.2:p.Ile1547Val
ENST00000460952.1:n.218A>G (STRC)
ENST00000471703.5:n.2593A>G (STRC)
ENST00000485556.5:n.3494A>G (STRC)
ENST00000493750.1:n.435A>G (STRC)
ENST00000541030.5:c.2320A>G (STRC)	ENSP00000440413.1:p.Ile774Val
NM_153700.2:c.4639A>G (STRC) MANE Select	NP_714544.1:p.Ile1547Val
XM_011521277.1:c.5128A>G (STRC)	XP_011519579.1:p.Ile1710Val
XM_011521278.1:c.4744A>G (STRC)	XP_011519580.1:p.Ile1582Val
XM_011521279.1:c.4744A>G (STRC)	XP_011519581.1:p.Ile1582Val