Canonical Allele Identifier: CA2483433185
Gene: CR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207523670G= , CM000663.2:g.207523670G= GRCh38
NC_000001.10:g.207697015G= , CM000663.1:g.207697015G= GRCh37
NC_000001.9:g.205763638G= NCBI36
NG_007481.1:g.32543G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367049.9:c.547G= MANE Select ENSP00000356016.4:p.Glu183=
ENST00000367051.6:c.487+12016G= ENSP00000356018.1:n.487+12016G=
ENST00000367052.6:c.547G= ENSP00000356019.1:p.Glu183=
ENST00000367053.6:c.547G= ENSP00000356020.1:p.Glu183=
ENST00000400960.7:c.547G= ENSP00000383744.2:p.Glu183=
ENST00000367049.8:c.547G= ENSP00000356016.4:p.Glu183=
ENST00000367050.8:n.668G=
ENST00000367051.5:c.487+12016G= ENSP00000356018.1:n.487+12016G=
ENST00000367052.5:c.547G= ENSP00000356019.1:p.Glu183=
ENST00000367053.5:c.547G= ENSP00000356020.1:p.Glu183=
ENST00000400960.6:c.547G= ENSP00000383744.2:p.Glu183=
ENST00000434033.5:n.474G=
ENST00000436595.1:n.414+12016G=
ENST00000450439.5:n.474G=
ENST00000529814.1:c.474G=
ENST00000534202.5:c.547G= ENSP00000436139.2:p.Glu183=
NM_000573.3:c.547G= NP_000564.2:p.Glu183=
NM_000651.4:c.547G= NP_000642.3:p.Glu183=
XM_006711166.2:c.562G= XP_006711229.1:p.Glu188=
XM_011509205.1:c.562G= XP_011507507.1:p.Glu188=
NM_000651.5:c.547G= NP_000642.3:p.Glu183=
XM_024453287.1:c.562G= XP_024309055.1:p.Glu188=
NM_000573.4:c.547G= NP_000564.2:p.Glu183=
NM_000651.6:c.547G= MANE Select NP_000642.3:p.Glu183=