Canonical Allele Identifier: CA1947210918

Gene: CDHR5

Linked Data

• dbSNP Id: rs1856927565

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.616862_616865del , CM000673.2:g.616862_616865del	GRCh38
NC_000011.9:g.616862_616865del , CM000673.1:g.616862_616865del	GRCh37
NC_000011.8:g.606862_606865del	NCBI36
NG_029106.1:g.4137_4140del

Transcript Alleles

HGVS	Amino-acid change
ENST00000358353.8:c.*488_*491del	ENSP00000351118.4:n.*488_*491del
ENST00000397542.7:c.*488_*491del MANE Select	ENSP00000380676.2:n.*488_*491del
ENST00000358353.7:c.*488_*491del	ENSP00000351118.3:n.*488_*491del
ENST00000397542.6:c.*488_*491del	ENSP00000380676.2:n.*488_*491del
NM_001171968.1:c.*488_*491del	NP_001165439.1:n.*488_*491del
NM_021924.4:c.*488_*491del	NP_068743.2:n.*488_*491del
NM_031264.3:c.*488_*491del	NP_112554.2:n.*488_*491del
XM_006718253.2:c.*488_*491del	XP_006718316.1:n.*488_*491del
XM_011520188.1:c.*488_*491del	XP_011518490.1:n.*488_*491del
XM_011520189.1:c.*488_*491del	XP_011518491.1:n.*488_*491del
XM_011520190.1:c.*703_*706del	XP_011518492.1:n.*703_*706del
XM_006718253.3:c.*488_*491del	XP_006718316.1:n.*488_*491del
XM_011520188.2:c.*488_*491del	XP_011518490.1:n.*488_*491del
XM_011520189.2:c.*488_*491del	XP_011518491.1:n.*488_*491del
XM_011520190.2:c.*703_*706del	XP_011518492.1:n.*703_*706del
NM_001171968.2:c.*488_*491del	NP_001165439.2:n.*488_*491del
NM_021924.5:c.*488_*491del MANE Select	NP_068743.3:n.*488_*491del
NM_031264.4:c.*488_*491del	NP_112554.3:n.*488_*491del
NM_001171968.3:c.*488_*491del	NP_001165439.2:n.*488_*491del
NM_031264.5:c.*488_*491del	NP_112554.3:n.*488_*491del