Canonical Allele Identifier: CA1947210737

Gene: CDHR5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.616781A= , CM000673.2:g.616781A=	GRCh38
NC_000011.9:g.616781A= , CM000673.1:g.616781A=	GRCh37
NC_000011.8:g.606781A=	NCBI36
NG_029106.1:g.4219T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000358353.8:c.*570T=	ENSP00000351118.4:n.*570T=
ENST00000397542.7:c.*570T= MANE Select	ENSP00000380676.2:n.*570T=
ENST00000358353.7:c.*570T=	ENSP00000351118.3:n.*570T=
ENST00000397542.6:c.*570T=	ENSP00000380676.2:n.*570T=
NM_001171968.1:c.*570T=	NP_001165439.1:n.*570T=
NM_021924.4:c.*570T=	NP_068743.2:n.*570T=
NM_031264.3:c.*570T=	NP_112554.2:n.*570T=
XM_006718253.2:c.*570T=	XP_006718316.1:n.*570T=
XM_011520188.1:c.*570T=	XP_011518490.1:n.*570T=
XM_011520189.1:c.*570T=	XP_011518491.1:n.*570T=
XM_011520190.1:c.*785T=	XP_011518492.1:n.*785T=
XM_006718253.3:c.*570T=	XP_006718316.1:n.*570T=
XM_011520188.2:c.*570T=	XP_011518490.1:n.*570T=
XM_011520189.2:c.*570T=	XP_011518491.1:n.*570T=
XM_011520190.2:c.*785T=	XP_011518492.1:n.*785T=
NM_001171968.2:c.*570T=	NP_001165439.2:n.*570T=
NM_021924.5:c.*570T= MANE Select	NP_068743.3:n.*570T=
NM_031264.4:c.*570T=	NP_112554.3:n.*570T=
NM_001171968.3:c.*570T=	NP_001165439.2:n.*570T=
NM_031264.5:c.*570T=	NP_112554.3:n.*570T=