Canonical Allele Identifier: CA392162618

Gene: STRC CKMT1B

Linked Data

• gnomAD v4: 15-43600891-T-C
• MyVariant Identifiers: chr15:g.43893089T>C (hg19) ; chr15:g.43600891T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43600891T>C , CM000677.2:g.43600891T>C	GRCh38
NC_000015.9:g.43893089T>C , CM000677.1:g.43893089T>C	GRCh37
NC_000015.8:g.41680381T>C	NCBI36
NG_011636.1:g.22910A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.4825A>G (STRC) MANE Select	ENSP00000401513.2:p.Ile1609Val
ENST00000411560.1:n.142+1358T>C (CKMT1B)
ENST00000428650.5:c.*1858A>G (STRC)	ENSP00000415991.1:n.*1858A>G
ENST00000440125.5:c.*2617A>G (STRC)	ENSP00000394866.1:n.*2617A>G
ENST00000448437.6:n.1945A>G (STRC)
ENST00000450892.6:c.4825A>G (STRC)	ENSP00000401513.2:p.Ile1609Val
ENST00000460952.1:n.404A>G (STRC)
ENST00000471703.5:n.2779A>G (STRC)
ENST00000485556.5:n.3680A>G (STRC)
ENST00000541030.5:c.2506A>G (STRC)	ENSP00000440413.1:p.Ile836Val
NM_153700.2:c.4825A>G (STRC) MANE Select	NP_714544.1:p.Ile1609Val
XM_011521277.1:c.5314A>G (STRC)	XP_011519579.1:p.Ile1772Val
XM_011521278.1:c.4930A>G (STRC)	XP_011519580.1:p.Ile1644Val
XM_011521279.1:c.4930A>G (STRC)	XP_011519581.1:p.Ile1644Val