Canonical Allele Identifier: CA2628140828

Gene: STRC CKMT1B

Linked Data

• gnomAD v4: 15-43599592-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43599592G>T , CM000677.2:g.43599592G>T	GRCh38
NC_000015.9:g.43891790G>T , CM000677.1:g.43891790G>T	GRCh37
NC_000015.8:g.41679082G>T	NCBI36
NG_011636.1:g.24209C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.*80C>A (STRC) MANE Select	ENSP00000401513.2:n.*80C>A
ENST00000411560.1:n.142+59G>T (CKMT1B)
ENST00000450892.6:c.*80C>A (STRC)	ENSP00000401513.2:n.*80C>A
ENST00000471703.5:n.3362C>A (STRC)
ENST00000541030.5:c.*80C>A (STRC)	ENSP00000440413.1:n.*80C>A
NM_153700.2:c.*80C>A (STRC) MANE Select	NP_714544.1:n.*80C>A
XM_011521277.1:c.*80C>A (STRC)	XP_011519579.1:n.*80C>A
XM_011521278.1:c.*80C>A (STRC)	XP_011519580.1:n.*80C>A
XM_011521279.1:c.*80C>A (STRC)	XP_011519581.1:n.*80C>A