Canonical Allele Identifier: CA2628141086

Gene: STRC CKMT1B

Linked Data

• gnomAD v4: 15-43604619-G-GT

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43604621dup , CM000677.2:g.43604621dup	GRCh38
NC_000015.9:g.43896819dup , CM000677.1:g.43896819dup	GRCh37
NC_000015.8:g.41684111dup	NCBI36
NG_011636.1:g.19181dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000450892.7:c.4127+30dup (STRC) MANE Select	ENSP00000401513.2:n.4127+30dup
ENST00000411560.1:n.143-163dup (CKMT1B)
ENST00000428650.5:c.*1330+30dup (STRC)	ENSP00000415991.1:n.*1330+30dup
ENST00000440125.5:c.*1919+30dup (STRC)	ENSP00000394866.1:n.*1919+30dup
ENST00000448437.6:n.1666-3069dup (STRC)
ENST00000450892.6:c.4127+30dup (STRC)	ENSP00000401513.2:n.4127+30dup
ENST00000471703.5:n.2081+30dup (STRC)
ENST00000485556.5:n.2982+30dup (STRC)
ENST00000541030.5:c.1808+30dup (STRC)	ENSP00000440413.1:n.1808+30dup
NM_153700.2:c.4127+30dup (STRC) MANE Select	NP_714544.1:n.4127+30dup
XM_011521277.1:c.4616+30dup (STRC)	XP_011519579.1:n.4616+30dup
XM_011521278.1:c.4232+30dup (STRC)	XP_011519580.1:n.4232+30dup
XM_011521279.1:c.4232+30dup (STRC)	XP_011519581.1:n.4232+30dup