Canonical Allele Identifier: CA2628141500

Gene: STRC CKMT1B

Linked Data

• gnomAD v4: 15-43600751-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43600751A>G , CM000677.2:g.43600751A>G	GRCh38
NC_000015.9:g.43892949A>G , CM000677.1:g.43892949A>G	GRCh37
NC_000015.8:g.41680241A>G	NCBI36
NG_011636.1:g.23050T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.4845-69T>C (STRC) MANE Select	ENSP00000401513.2:n.4845-69T>C
ENST00000411560.1:n.142+1218A>G (CKMT1B)
ENST00000428650.5:c.*1878-69T>C (STRC)	ENSP00000415991.1:n.*1878-69T>C
ENST00000440125.5:c.*2637-69T>C (STRC)	ENSP00000394866.1:n.*2637-69T>C
ENST00000448437.6:n.1965-69T>C (STRC)
ENST00000450892.6:c.4845-69T>C (STRC)	ENSP00000401513.2:n.4845-69T>C
ENST00000460952.1:n.424-69T>C (STRC)
ENST00000471703.5:n.2799-69T>C (STRC)
ENST00000485556.5:n.3700-69T>C (STRC)
ENST00000541030.5:c.2526-69T>C (STRC)	ENSP00000440413.1:n.2526-69T>C
NM_153700.2:c.4845-69T>C (STRC) MANE Select	NP_714544.1:n.4845-69T>C
XM_011521277.1:c.5334-69T>C (STRC)	XP_011519579.1:n.5334-69T>C
XM_011521278.1:c.4950-69T>C (STRC)	XP_011519580.1:n.4950-69T>C
XM_011521279.1:c.4950-69T>C (STRC)	XP_011519581.1:n.4950-69T>C