Canonical Allele Identifier: CA1947220589

Gene: CDHR5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.620599G= , CM000673.2:g.620599G=	GRCh38
NC_000011.9:g.620599G= , CM000673.1:g.620599G=	GRCh37
NC_000011.8:g.610599G=	NCBI36
NG_029106.1:g.401C=

Transcript Alleles

HGVS	Amino-acid Change
NM_021924.5:c.790-213C= MANE Select	NP_068743.3:n.790-213C=
ENST00000397542.7:c.790-213C= MANE Select	ENSP00000380676.2:n.790-213C=
NM_001171968.1:c.790-213C=	NP_001165439.1:n.790-213C=
NM_001171968.2:c.790-213C=	NP_001165439.2:n.790-213C=
NM_001171968.3:c.790-213C=	NP_001165439.2:n.790-213C=
NM_021924.4:c.790-213C=	NP_068743.2:n.790-213C=
NM_031264.3:c.790-213C=	NP_112554.2:n.790-213C=
NM_031264.4:c.790-213C=	NP_112554.3:n.790-213C=
NM_031264.5:c.790-213C=	NP_112554.3:n.790-213C=
ENST00000349570.11:c.790-213C=	ENSP00000345726.7:n.790-213C=
ENST00000358353.7:c.790-213C=	ENSP00000351118.3:n.790-213C=
ENST00000358353.8:c.790-213C=	ENSP00000351118.4:n.790-213C=
ENST00000397542.6:c.790-213C=	ENSP00000380676.2:n.790-213C=
ENST00000531177.5:c.*622-213C=	ENSP00000437255.1:n.*622-213C=
ENST00000531899.5:n.750-213C=
ENST00000532949.1:n.59-213C=
ENST00000674088.1:c.790-213C=	ENSP00000501074.1:n.790-213C=
XM_006718253.2:c.790-213C=	XP_006718316.1:n.790-213C=
XM_006718253.3:c.790-213C=	XP_006718316.1:n.790-213C=
XM_011520188.1:c.790-213C=	XP_011518490.1:n.790-213C=
XM_011520188.2:c.790-213C=	XP_011518490.1:n.790-213C=
XM_011520189.1:c.790-213C=	XP_011518491.1:n.790-213C=
XM_011520189.2:c.790-213C=	XP_011518491.1:n.790-213C=
XM_011520190.1:c.790-213C=	XP_011518492.1:n.790-213C=
XM_011520190.2:c.790-213C=	XP_011518492.1:n.790-213C=
XM_011520191.1:c.790-213C=	XP_011518493.1:n.790-213C=
XM_011520191.2:c.790-213C=	XP_011518493.1:n.790-213C=
XM_024448584.1:c.790-213C=	XP_024304352.1:n.790-213C=