Canonical Allele Identifier: CA2739364170

Gene: CDHR5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.616857C>G , CM000673.2:g.616857C>G	GRCh38
NC_000011.9:g.616857C>G , CM000673.1:g.616857C>G	GRCh37
NC_000011.8:g.606857C>G	NCBI36
NG_029106.1:g.4143G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358353.8:c.*494G>C	ENSP00000351118.4:n.*494G>C
ENST00000397542.7:c.*494G>C MANE Select	ENSP00000380676.2:n.*494G>C
ENST00000358353.7:c.*494G>C	ENSP00000351118.3:n.*494G>C
ENST00000397542.6:c.*494G>C	ENSP00000380676.2:n.*494G>C
NM_001171968.1:c.*494G>C	NP_001165439.1:n.*494G>C
NM_021924.4:c.*494G>C	NP_068743.2:n.*494G>C
NM_031264.3:c.*494G>C	NP_112554.2:n.*494G>C
XM_006718253.2:c.*494G>C	XP_006718316.1:n.*494G>C
XM_011520188.1:c.*494G>C	XP_011518490.1:n.*494G>C
XM_011520189.1:c.*494G>C	XP_011518491.1:n.*494G>C
XM_011520190.1:c.*709G>C	XP_011518492.1:n.*709G>C
XM_006718253.3:c.*494G>C	XP_006718316.1:n.*494G>C
XM_011520188.2:c.*494G>C	XP_011518490.1:n.*494G>C
XM_011520189.2:c.*494G>C	XP_011518491.1:n.*494G>C
XM_011520190.2:c.*709G>C	XP_011518492.1:n.*709G>C
NM_001171968.2:c.*494G>C	NP_001165439.2:n.*494G>C
NM_021924.5:c.*494G>C MANE Select	NP_068743.3:n.*494G>C
NM_031264.4:c.*494G>C	NP_112554.3:n.*494G>C
NM_001171968.3:c.*494G>C	NP_001165439.2:n.*494G>C
NM_031264.5:c.*494G>C	NP_112554.3:n.*494G>C