Canonical Allele Identifier: CA1141837493
Gene: CR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207580298C= , CM000663.2:g.207580298C= GRCh38
NC_000001.10:g.207753643C= , CM000663.1:g.207753643C= GRCh37
NC_000001.9:g.205820266C= NCBI36
NG_007481.1:g.89171C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367049.9:c.4995C= MANE Select ENSP00000356016.4:p.Asn1665=
ENST00000367051.6:c.3645C= ENSP00000356018.1:p.Asn1215=
ENST00000367052.6:c.3645C= ENSP00000356019.1:p.Asn1215=
ENST00000367053.6:c.3645C= ENSP00000356020.1:p.Asn1215=
ENST00000400960.7:c.3645C= ENSP00000383744.2:p.Asn1215=
ENST00000367049.8:c.4995C= ENSP00000356016.4:p.Asn1665=
ENST00000367051.5:c.3645C= ENSP00000356018.1:p.Asn1215=
ENST00000367052.5:c.3645C= ENSP00000356019.1:p.Asn1215=
ENST00000367053.5:c.3645C= ENSP00000356020.1:p.Asn1215=
ENST00000400960.6:c.3645C= ENSP00000383744.2:p.Asn1215=
ENST00000529814.1:c.1179+14375C=
ENST00000534202.5:c.*760C= ENSP00000436139.2:n.*760C=
NM_000573.3:c.3645C= NP_000564.2:p.Asn1215=
NM_000651.4:c.4995C= NP_000642.3:p.Asn1665=
XM_006711166.2:c.5010C= XP_006711229.1:p.Asn1670=
XM_011509205.1:c.5010C= XP_011507507.1:p.Asn1670=
NM_000651.5:c.4995C= NP_000642.3:p.Asn1665=
XM_024453287.1:c.3660C= XP_024309055.1:p.Asn1220=
NM_000573.4:c.3645C= NP_000564.2:p.Asn1215=
NM_000651.6:c.4995C= MANE Select NP_000642.3:p.Asn1665=