Canonical Allele Identifier: CA2628141007

Gene: STRC CKMT1B

Linked Data

• gnomAD v4: 15-43599901-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43599901T>G , CM000677.2:g.43599901T>G	GRCh38
NC_000015.9:g.43892099T>G , CM000677.1:g.43892099T>G	GRCh37
NC_000015.8:g.41679391T>G	NCBI36
NG_011636.1:g.23900A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.5239+59A>C (STRC) MANE Select	ENSP00000401513.2:n.5239+59A>C
ENST00000411560.1:n.142+368T>G (CKMT1B)
ENST00000428650.5:c.*2272+59A>C (STRC)	ENSP00000415991.1:n.*2272+59A>C
ENST00000440125.5:c.*3031+59A>C (STRC)	ENSP00000394866.1:n.*3031+59A>C
ENST00000448437.6:n.2359+59A>C (STRC)
ENST00000450892.6:c.5239+59A>C (STRC)	ENSP00000401513.2:n.5239+59A>C
ENST00000471703.5:n.3193+59A>C (STRC)
ENST00000485556.5:n.4094+59A>C (STRC)
ENST00000541030.5:c.2920+59A>C (STRC)	ENSP00000440413.1:n.2920+59A>C
NM_153700.2:c.5239+59A>C (STRC) MANE Select	NP_714544.1:n.5239+59A>C
XM_011521277.1:c.5728+59A>C (STRC)	XP_011519579.1:n.5728+59A>C
XM_011521278.1:c.5344+59A>C (STRC)	XP_011519580.1:n.5344+59A>C
XM_011521279.1:c.5344+59A>C (STRC)	XP_011519581.1:n.5344+59A>C