Canonical Allele Identifier: CA1369483
Gene: CR1 HGNC NCBI

Linked Data

dbSNP Id: rs769263469

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207523800G>C , CM000663.2:g.207523800G>C GRCh38
NC_000001.10:g.207697145G>C , CM000663.1:g.207697145G>C GRCh37
NC_000001.9:g.205763768G>C NCBI36
NG_007481.1:g.32673G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367049.9:c.677G>C MANE Select ENSP00000356016.4:p.Ser226Thr
ENST00000367051.6:c.487+12146G>C ENSP00000356018.1:n.487+12146G>C
ENST00000367052.6:c.677G>C ENSP00000356019.1:p.Ser226Thr
ENST00000367053.6:c.677G>C ENSP00000356020.1:p.Ser226Thr
ENST00000400960.7:c.677G>C ENSP00000383744.2:p.Ser226Thr
ENST00000367049.8:c.677G>C ENSP00000356016.4:p.Ser226Thr
ENST00000367050.8:n.798G>C
ENST00000367051.5:c.487+12146G>C ENSP00000356018.1:n.487+12146G>C
ENST00000367052.5:c.677G>C ENSP00000356019.1:p.Ser226Thr
ENST00000367053.5:c.677G>C ENSP00000356020.1:p.Ser226Thr
ENST00000400960.6:c.677G>C ENSP00000383744.2:p.Ser226Thr
ENST00000434033.5:n.604G>C
ENST00000436595.1:n.414+12146G>C
ENST00000450439.5:n.604G>C
ENST00000529814.1:c.604G>C
ENST00000534202.5:c.677G>C ENSP00000436139.2:p.Ser226Thr
NM_000573.3:c.677G>C NP_000564.2:p.Ser226Thr
NM_000651.4:c.677G>C NP_000642.3:p.Ser226Thr
XM_006711166.2:c.692G>C XP_006711229.1:p.Ser231Thr
XM_011509205.1:c.692G>C XP_011507507.1:p.Ser231Thr
NM_000651.5:c.677G>C NP_000642.3:p.Ser226Thr
XM_024453287.1:c.692G>C XP_024309055.1:p.Ser231Thr
NM_000573.4:c.677G>C NP_000564.2:p.Ser226Thr
NM_000651.6:c.677G>C MANE Select NP_000642.3:p.Ser226Thr