Canonical Allele Identifier: CA1947210979

Gene: CDHR5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.616865G= , CM000673.2:g.616865G=	GRCh38
NC_000011.9:g.616865G= , CM000673.1:g.616865G=	GRCh37
NC_000011.8:g.606865G=	NCBI36
NG_029106.1:g.4135C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358353.8:c.*486C=	ENSP00000351118.4:n.*486C=
ENST00000397542.7:c.*486C= MANE Select	ENSP00000380676.2:n.*486C=
ENST00000358353.7:c.*486C=	ENSP00000351118.3:n.*486C=
ENST00000397542.6:c.*486C=	ENSP00000380676.2:n.*486C=
NM_001171968.1:c.*486C=	NP_001165439.1:n.*486C=
NM_021924.4:c.*486C=	NP_068743.2:n.*486C=
NM_031264.3:c.*486C=	NP_112554.2:n.*486C=
XM_006718253.2:c.*486C=	XP_006718316.1:n.*486C=
XM_011520188.1:c.*486C=	XP_011518490.1:n.*486C=
XM_011520189.1:c.*486C=	XP_011518491.1:n.*486C=
XM_011520190.1:c.*701C=	XP_011518492.1:n.*701C=
XM_006718253.3:c.*486C=	XP_006718316.1:n.*486C=
XM_011520188.2:c.*486C=	XP_011518490.1:n.*486C=
XM_011520189.2:c.*486C=	XP_011518491.1:n.*486C=
XM_011520190.2:c.*701C=	XP_011518492.1:n.*701C=
NM_001171968.2:c.*486C=	NP_001165439.2:n.*486C=
NM_021924.5:c.*486C= MANE Select	NP_068743.3:n.*486C=
NM_031264.4:c.*486C=	NP_112554.3:n.*486C=
NM_001171968.3:c.*486C=	NP_001165439.2:n.*486C=
NM_031264.5:c.*486C=	NP_112554.3:n.*486C=