Canonical Allele Identifier: CA2628141088

Gene: STRC CKMT1B

Linked Data

• gnomAD v4: 15-43604625-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43604625A>G , CM000677.2:g.43604625A>G	GRCh38
NC_000015.9:g.43896823A>G , CM000677.1:g.43896823A>G	GRCh37
NC_000015.8:g.41684115A>G	NCBI36
NG_011636.1:g.19176T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.4127+25T>C (STRC) MANE Select	ENSP00000401513.2:n.4127+25T>C
ENST00000411560.1:n.143-159A>G (CKMT1B)
ENST00000428650.5:c.*1330+25T>C (STRC)	ENSP00000415991.1:n.*1330+25T>C
ENST00000440125.5:c.*1919+25T>C (STRC)	ENSP00000394866.1:n.*1919+25T>C
ENST00000448437.6:n.1666-3074T>C (STRC)
ENST00000450892.6:c.4127+25T>C (STRC)	ENSP00000401513.2:n.4127+25T>C
ENST00000471703.5:n.2081+25T>C (STRC)
ENST00000485556.5:n.2982+25T>C (STRC)
ENST00000541030.5:c.1808+25T>C (STRC)	ENSP00000440413.1:n.1808+25T>C
NM_153700.2:c.4127+25T>C (STRC) MANE Select	NP_714544.1:n.4127+25T>C
XM_011521277.1:c.4616+25T>C (STRC)	XP_011519579.1:n.4616+25T>C
XM_011521278.1:c.4232+25T>C (STRC)	XP_011519580.1:n.4232+25T>C
XM_011521279.1:c.4232+25T>C (STRC)	XP_011519581.1:n.4232+25T>C