Canonical Allele Identifier: CA2628140938

Gene: STRC CKMT1B

Linked Data

• gnomAD v4: 15-43599846-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43599846C>T , CM000677.2:g.43599846C>T	GRCh38
NC_000015.9:g.43892044C>T , CM000677.1:g.43892044C>T	GRCh37
NC_000015.8:g.41679336C>T	NCBI36
NG_011636.1:g.23955G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.5240-86G>A (STRC) MANE Select	ENSP00000401513.2:n.5240-86G>A
ENST00000411560.1:n.142+313C>T (CKMT1B)
ENST00000428650.5:c.*2273-86G>A (STRC)	ENSP00000415991.1:n.*2273-86G>A
ENST00000440125.5:c.*3032-86G>A (STRC)	ENSP00000394866.1:n.*3032-86G>A
ENST00000448437.6:n.2360-86G>A (STRC)
ENST00000450892.6:c.5240-86G>A (STRC)	ENSP00000401513.2:n.5240-86G>A
ENST00000471703.5:n.3194-86G>A (STRC)
ENST00000485556.5:n.4095-86G>A (STRC)
ENST00000541030.5:c.2921-86G>A (STRC)	ENSP00000440413.1:n.2921-86G>A
NM_153700.2:c.5240-86G>A (STRC) MANE Select	NP_714544.1:n.5240-86G>A
XM_011521277.1:c.5729-86G>A (STRC)	XP_011519579.1:n.5729-86G>A
XM_011521278.1:c.5345-86G>A (STRC)	XP_011519580.1:n.5345-86G>A
XM_011521279.1:c.5345-86G>A (STRC)	XP_011519581.1:n.5345-86G>A