Canonical Allele Identifier: CA1947211208

Gene: CDHR5

Linked Data

• dbSNP Id: rs1856936504
• gnomAD v4: 11-616954-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.616954G>T , CM000673.2:g.616954G>T	GRCh38
NC_000011.9:g.616954G>T , CM000673.1:g.616954G>T	GRCh37
NC_000011.8:g.606954G>T	NCBI36
NG_029106.1:g.4046C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358353.8:c.*397C>A	ENSP00000351118.4:n.*397C>A
ENST00000397542.7:c.*397C>A MANE Select	ENSP00000380676.2:n.*397C>A
ENST00000358353.7:c.*397C>A	ENSP00000351118.3:n.*397C>A
ENST00000397542.6:c.*397C>A	ENSP00000380676.2:n.*397C>A
NM_001171968.1:c.*397C>A	NP_001165439.1:n.*397C>A
NM_021924.4:c.*397C>A	NP_068743.2:n.*397C>A
NM_031264.3:c.*397C>A	NP_112554.2:n.*397C>A
XM_006718253.2:c.*397C>A	XP_006718316.1:n.*397C>A
XM_011520188.1:c.*397C>A	XP_011518490.1:n.*397C>A
XM_011520189.1:c.*397C>A	XP_011518491.1:n.*397C>A
XM_011520190.1:c.*612C>A	XP_011518492.1:n.*612C>A
XM_006718253.3:c.*397C>A	XP_006718316.1:n.*397C>A
XM_011520188.2:c.*397C>A	XP_011518490.1:n.*397C>A
XM_011520189.2:c.*397C>A	XP_011518491.1:n.*397C>A
XM_011520190.2:c.*612C>A	XP_011518492.1:n.*612C>A
NM_001171968.2:c.*397C>A	NP_001165439.2:n.*397C>A
NM_021924.5:c.*397C>A MANE Select	NP_068743.3:n.*397C>A
NM_031264.4:c.*397C>A	NP_112554.3:n.*397C>A
NM_001171968.3:c.*397C>A	NP_001165439.2:n.*397C>A
NM_031264.5:c.*397C>A	NP_112554.3:n.*397C>A