Canonical Allele Identifier: CA712990165

Gene: STRC CKMT1B

Linked Data

• dbSNP Id: rs1168641910
• gnomAD v3: 15-43600814-T-C
• gnomAD v4: 15-43600814-T-C
• MyVariant Identifiers: chr15:g.43893012T>C (hg19) ; chr15:g.43600814T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43600814T>C , CM000677.2:g.43600814T>C	GRCh38
NC_000015.9:g.43893012T>C , CM000677.1:g.43893012T>C	GRCh37
NC_000015.8:g.41680304T>C	NCBI36
NG_011636.1:g.22987A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.4844+58A>G (STRC) MANE Select	ENSP00000401513.2:n.4844+58A>G
ENST00000411560.1:n.142+1281T>C (CKMT1B)
ENST00000428650.5:c.*1877+58A>G (STRC)	ENSP00000415991.1:n.*1877+58A>G
ENST00000440125.5:c.*2636+58A>G (STRC)	ENSP00000394866.1:n.*2636+58A>G
ENST00000448437.6:n.1964+58A>G (STRC)
ENST00000450892.6:c.4844+58A>G (STRC)	ENSP00000401513.2:n.4844+58A>G
ENST00000460952.1:n.423+58A>G (STRC)
ENST00000471703.5:n.2798+58A>G (STRC)
ENST00000485556.5:n.3699+58A>G (STRC)
ENST00000541030.5:c.2525+58A>G (STRC)	ENSP00000440413.1:n.2525+58A>G
NM_153700.2:c.4844+58A>G (STRC) MANE Select	NP_714544.1:n.4844+58A>G
XM_011521277.1:c.5333+58A>G (STRC)	XP_011519579.1:n.5333+58A>G
XM_011521278.1:c.4949+58A>G (STRC)	XP_011519580.1:n.4949+58A>G
XM_011521279.1:c.4949+58A>G (STRC)	XP_011519581.1:n.4949+58A>G