Canonical Allele Identifier: CA2628141018

Gene: STRC CKMT1B

Linked Data

• gnomAD v4: 15-43599918-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43599918G>T , CM000677.2:g.43599918G>T	GRCh38
NC_000015.9:g.43892116G>T , CM000677.1:g.43892116G>T	GRCh37
NC_000015.8:g.41679408G>T	NCBI36
NG_011636.1:g.23883C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.5239+42C>A (STRC) MANE Select	ENSP00000401513.2:n.5239+42C>A
ENST00000411560.1:n.142+385G>T (CKMT1B)
ENST00000428650.5:c.*2272+42C>A (STRC)	ENSP00000415991.1:n.*2272+42C>A
ENST00000440125.5:c.*3031+42C>A (STRC)	ENSP00000394866.1:n.*3031+42C>A
ENST00000448437.6:n.2359+42C>A (STRC)
ENST00000450892.6:c.5239+42C>A (STRC)	ENSP00000401513.2:n.5239+42C>A
ENST00000471703.5:n.3193+42C>A (STRC)
ENST00000485556.5:n.4094+42C>A (STRC)
ENST00000541030.5:c.2920+42C>A (STRC)	ENSP00000440413.1:n.2920+42C>A
NM_153700.2:c.5239+42C>A (STRC) MANE Select	NP_714544.1:n.5239+42C>A
XM_011521277.1:c.5728+42C>A (STRC)	XP_011519579.1:n.5728+42C>A
XM_011521278.1:c.5344+42C>A (STRC)	XP_011519580.1:n.5344+42C>A
XM_011521279.1:c.5344+42C>A (STRC)	XP_011519581.1:n.5344+42C>A