Canonical Allele Identifier: CA2173247672

Gene: CKMT1B STRC

Linked Data

• dbSNP Id: rs2085646029

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43599416_43599417del , CM000677.2:g.43599416_43599417del	GRCh38
NC_000015.9:g.43891614_43891615del , CM000677.1:g.43891614_43891615del	GRCh37
NC_000015.8:g.41678906_41678907del	NCBI36
NG_011636.1:g.24387_24388del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411560.1:n.25_26del (CKMT1B)
ENST00000450892.6:c.*258_*259del (STRC)	ENSP00000401513.2:n.*258_*259del
XM_011521277.1:c.*258_*259del (STRC)	XP_011519579.1:n.*258_*259del
XM_011521278.1:c.*258_*259del (STRC)	XP_011519580.1:n.*258_*259del
XM_011521279.1:c.*258_*259del (STRC)	XP_011519581.1:n.*258_*259del