Canonical Allele Identifier: CA2628142648

Gene: STRC CKMT1B

Linked Data

• gnomAD v4: 15-43601613-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43601613G>A , CM000677.2:g.43601613G>A	GRCh38
NC_000015.9:g.43893811G>A , CM000677.1:g.43893811G>A	GRCh37
NC_000015.8:g.41681103G>A	NCBI36
NG_011636.1:g.22188C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.4546-62C>T (STRC) MANE Select	ENSP00000401513.2:n.4546-62C>T
ENST00000411560.1:n.142+2080G>A (CKMT1B)
ENST00000428650.5:c.*1579-62C>T (STRC)	ENSP00000415991.1:n.*1579-62C>T
ENST00000440125.5:c.*2338-62C>T (STRC)	ENSP00000394866.1:n.*2338-62C>T
ENST00000448437.6:n.1666-62C>T (STRC)
ENST00000450892.6:c.4546-62C>T (STRC)	ENSP00000401513.2:n.4546-62C>T
ENST00000460952.1:n.63C>T (STRC)
ENST00000471703.5:n.2500-62C>T (STRC)
ENST00000485556.5:n.3401-62C>T (STRC)
ENST00000493750.1:n.342-62C>T (STRC)
ENST00000541030.5:c.2227-62C>T (STRC)	ENSP00000440413.1:n.2227-62C>T
NM_153700.2:c.4546-62C>T (STRC) MANE Select	NP_714544.1:n.4546-62C>T
XM_011521277.1:c.5035-62C>T (STRC)	XP_011519579.1:n.5035-62C>T
XM_011521278.1:c.4651-62C>T (STRC)	XP_011519580.1:n.4651-62C>T
XM_011521279.1:c.4651-62C>T (STRC)	XP_011519581.1:n.4651-62C>T