Canonical Allele Identifier: CA2526336437
Gene: CR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207523573_207523580dup , CM000663.2:g.207523573_207523580dup GRCh38
NC_000001.10:g.207696918_207696925dup , CM000663.1:g.207696918_207696925dup GRCh37
NC_000001.9:g.205763541_205763548dup NCBI36
NG_007481.1:g.32446_32453dup

Transcript Alleles

HGVS Amino-acid change
ENST00000367049.9:c.488-38_488-31dup MANE Select ENSP00000356016.4:n.488-38_488-31dup
ENST00000367051.6:c.487+11919_487+11926dup ENSP00000356018.1:n.487+11919_487+11926dup
ENST00000367052.6:c.488-38_488-31dup ENSP00000356019.1:n.488-38_488-31dup
ENST00000367053.6:c.488-38_488-31dup ENSP00000356020.1:n.488-38_488-31dup
ENST00000400960.7:c.488-38_488-31dup ENSP00000383744.2:n.488-38_488-31dup
ENST00000367049.8:c.488-38_488-31dup ENSP00000356016.4:n.488-38_488-31dup
ENST00000367050.8:n.609-38_609-31dup
ENST00000367051.5:c.487+11919_487+11926dup ENSP00000356018.1:n.487+11919_487+11926dup
ENST00000367052.5:c.488-38_488-31dup ENSP00000356019.1:n.488-38_488-31dup
ENST00000367053.5:c.488-38_488-31dup ENSP00000356020.1:n.488-38_488-31dup
ENST00000400960.6:c.488-38_488-31dup ENSP00000383744.2:n.488-38_488-31dup
ENST00000434033.5:n.415-38_415-31dup
ENST00000436595.1:n.414+11919_414+11926dup
ENST00000450439.5:n.415-38_415-31dup
ENST00000529814.1:c.415-38_415-31dup
ENST00000534202.5:c.488-38_488-31dup ENSP00000436139.2:n.488-38_488-31dup
NM_000573.3:c.488-38_488-31dup NP_000564.2:n.488-38_488-31dup
NM_000651.4:c.488-38_488-31dup NP_000642.3:n.488-38_488-31dup
XM_006711166.2:c.503-38_503-31dup XP_006711229.1:n.503-38_503-31dup
XM_011509205.1:c.503-38_503-31dup XP_011507507.1:n.503-38_503-31dup
NM_000651.5:c.488-38_488-31dup NP_000642.3:n.488-38_488-31dup
XM_024453287.1:c.503-38_503-31dup XP_024309055.1:n.503-38_503-31dup
NM_000573.4:c.488-38_488-31dup NP_000564.2:n.488-38_488-31dup
NM_000651.6:c.488-38_488-31dup MANE Select NP_000642.3:n.488-38_488-31dup