Canonical Allele Identifier: CA1145894192
Gene: CR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207630830G= , CM000663.2:g.207630830G= GRCh38
NC_000001.10:g.207804175G= , CM000663.1:g.207804175G= GRCh37
NC_000001.9:g.205870798G= NCBI36
NG_007481.1:g.139703G=

Transcript Alleles

HGVS Amino-acid change
ENST00000367049.9:c.7457+209G= MANE Select ENSP00000356016.4:n.7457+209G=
ENST00000367051.6:c.6107+209G= ENSP00000356018.1:n.6107+209G=
ENST00000367052.6:c.6107+209G= ENSP00000356019.1:n.6107+209G=
ENST00000367053.6:c.6107+209G= ENSP00000356020.1:n.6107+209G=
ENST00000400960.7:c.6107+209G= ENSP00000383744.2:n.6107+209G=
ENST00000367049.8:c.7457+209G= ENSP00000356016.4:n.7457+209G=
ENST00000367051.5:c.6107+209G= ENSP00000356018.1:n.6107+209G=
ENST00000367052.5:c.6107+209G= ENSP00000356019.1:n.6107+209G=
ENST00000367053.5:c.6107+209G= ENSP00000356020.1:n.6107+209G=
ENST00000400960.6:c.6107+209G= ENSP00000383744.2:n.6107+209G=
NM_000573.3:c.6107+209G= NP_000564.2:n.6107+209G=
NM_000651.4:c.7457+209G= NP_000642.3:n.7457+209G=
XM_006711166.2:c.7367+7762G= XP_006711229.1:n.7367+7762G=
XM_011509205.1:c.7472+209G= XP_011507507.1:n.7472+209G=
NM_000651.5:c.7457+209G= NP_000642.3:n.7457+209G=
XM_024453287.1:c.6122+209G= XP_024309055.1:n.6122+209G=
NM_000573.4:c.6107+209G= NP_000564.2:n.6107+209G=
NM_000651.6:c.7457+209G= MANE Select NP_000642.3:n.7457+209G=