Canonical Allele Identifier: CA216915477

Gene: CDHR5

Linked Data

• dbSNP Id: rs575998629
• gnomAD v3: 11-616717-CCCCTAGG-C
• gnomAD v4: 11-616717-CCCCTAGG-C
• MyVariant Identifiers: chr11:g.616718_616724del (hg19) ; chr11:g.616718_616724del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.616720_616726del , CM000673.2:g.616720_616726del	GRCh38
NC_000011.9:g.616720_616726del , CM000673.1:g.616720_616726del	GRCh37
NC_000011.8:g.606720_606726del	NCBI36
NG_029106.1:g.4276_4282del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358353.8:c.*627_*633del	ENSP00000351118.4:n.*627_*633del
ENST00000397542.7:c.*627_*633del MANE Select	ENSP00000380676.2:n.*627_*633del
ENST00000358353.7:c.*627_*633del	ENSP00000351118.3:n.*627_*633del
ENST00000397542.6:c.*627_*633del	ENSP00000380676.2:n.*627_*633del
NM_001171968.1:c.*627_*633del	NP_001165439.1:n.*627_*633del
NM_021924.4:c.*627_*633del	NP_068743.2:n.*627_*633del
NM_031264.3:c.*627_*633del	NP_112554.2:n.*627_*633del
XM_006718253.2:c.*627_*633del	XP_006718316.1:n.*627_*633del
XM_011520188.1:c.*627_*633del	XP_011518490.1:n.*627_*633del
XM_011520189.1:c.*627_*633del	XP_011518491.1:n.*627_*633del
XM_011520190.1:c.*842_*848del	XP_011518492.1:n.*842_*848del
XM_006718253.3:c.*627_*633del	XP_006718316.1:n.*627_*633del
XM_011520188.2:c.*627_*633del	XP_011518490.1:n.*627_*633del
XM_011520189.2:c.*627_*633del	XP_011518491.1:n.*627_*633del
XM_011520190.2:c.*842_*848del	XP_011518492.1:n.*842_*848del
NM_001171968.2:c.*627_*633del	NP_001165439.2:n.*627_*633del
NM_021924.5:c.*627_*633del MANE Select	NP_068743.3:n.*627_*633del
NM_031264.4:c.*627_*633del	NP_112554.3:n.*627_*633del
NM_001171968.3:c.*627_*633del	NP_001165439.2:n.*627_*633del
NM_031264.5:c.*627_*633del	NP_112554.3:n.*627_*633del