Canonical Allele Identifier: CA2628140959

Gene: STRC CKMT1B

Linked Data

• gnomAD v4: 15-43604320-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43604320C>A , CM000677.2:g.43604320C>A	GRCh38
NC_000015.9:g.43896518C>A , CM000677.1:g.43896518C>A	GRCh37
NC_000015.8:g.41683810C>A	NCBI36
NG_011636.1:g.19481G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.4218+41G>T (STRC) MANE Select	ENSP00000401513.2:n.4218+41G>T
ENST00000411560.1:n.143-464C>A (CKMT1B)
ENST00000428650.5:c.*1421+41G>T (STRC)	ENSP00000415991.1:n.*1421+41G>T
ENST00000440125.5:c.*2010+41G>T (STRC)	ENSP00000394866.1:n.*2010+41G>T
ENST00000448437.6:n.1666-2769G>T (STRC)
ENST00000450892.6:c.4218+41G>T (STRC)	ENSP00000401513.2:n.4218+41G>T
ENST00000471703.5:n.2172+41G>T (STRC)
ENST00000485556.5:n.3073+41G>T (STRC)
ENST00000541030.5:c.1899+41G>T (STRC)	ENSP00000440413.1:n.1899+41G>T
NM_153700.2:c.4218+41G>T (STRC) MANE Select	NP_714544.1:n.4218+41G>T
XM_011521277.1:c.4707+41G>T (STRC)	XP_011519579.1:n.4707+41G>T
XM_011521278.1:c.4323+41G>T (STRC)	XP_011519580.1:n.4323+41G>T
XM_011521279.1:c.4323+41G>T (STRC)	XP_011519581.1:n.4323+41G>T