Canonical Allele Identifier: CA2483464785
Gene: CR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207630806G= , CM000663.2:g.207630806G= GRCh38
NC_000001.10:g.207804151G= , CM000663.1:g.207804151G= GRCh37
NC_000001.9:g.205870774G= NCBI36
NG_007481.1:g.139679G=

Transcript Alleles

HGVS Amino-acid change
ENST00000367049.9:c.7457+185G= MANE Select ENSP00000356016.4:n.7457+185G=
ENST00000367051.6:c.6107+185G= ENSP00000356018.1:n.6107+185G=
ENST00000367052.6:c.6107+185G= ENSP00000356019.1:n.6107+185G=
ENST00000367053.6:c.6107+185G= ENSP00000356020.1:n.6107+185G=
ENST00000400960.7:c.6107+185G= ENSP00000383744.2:n.6107+185G=
ENST00000367049.8:c.7457+185G= ENSP00000356016.4:n.7457+185G=
ENST00000367051.5:c.6107+185G= ENSP00000356018.1:n.6107+185G=
ENST00000367052.5:c.6107+185G= ENSP00000356019.1:n.6107+185G=
ENST00000367053.5:c.6107+185G= ENSP00000356020.1:n.6107+185G=
ENST00000400960.6:c.6107+185G= ENSP00000383744.2:n.6107+185G=
NM_000573.3:c.6107+185G= NP_000564.2:n.6107+185G=
NM_000651.4:c.7457+185G= NP_000642.3:n.7457+185G=
XM_006711166.2:c.7367+7738G= XP_006711229.1:n.7367+7738G=
XM_011509205.1:c.7472+185G= XP_011507507.1:n.7472+185G=
NM_000651.5:c.7457+185G= NP_000642.3:n.7457+185G=
XM_024453287.1:c.6122+185G= XP_024309055.1:n.6122+185G=
NM_000573.4:c.6107+185G= NP_000564.2:n.6107+185G=
NM_000651.6:c.7457+185G= MANE Select NP_000642.3:n.7457+185G=