Canonical Allele Identifier: CA2483456588

Gene: CR1

Linked Data

• dbSNP Id: rs541502141

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207611854_207611870dup , CM000663.2:g.207611854_207611870dup	GRCh38
NC_000001.10:g.207785199_207785215dup , CM000663.1:g.207785199_207785215dup	GRCh37
NC_000001.9:g.205851822_205851838dup	NCBI36
NG_007481.1:g.120727_120743dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367049.9:c.6472+1_6472+17dup
ENST00000367051.6:c.5122+1_5122+17dup
ENST00000367052.6:c.5122+1_5122+17dup
ENST00000367053.6:c.5122+1_5122+17dup
ENST00000400960.7:c.5122+1_5122+17dup
ENST00000367049.8:c.6472+1_6472+17dup
ENST00000367051.5:c.5122+1_5122+17dup
ENST00000367052.5:c.5122+1_5122+17dup
ENST00000367053.5:c.5122+1_5122+17dup
ENST00000400960.6:c.5122+1_5122+17dup
ENST00000529814.1:c.1180-4721_1180-4705dup
NM_000573.3:c.5122+1_5122+17dup
NM_000651.4:c.6472+1_6472+17dup
XM_006711166.2:c.6487+1_6487+17dup
XM_011509205.1:c.6487+1_6487+17dup
NM_000651.5:c.6472+1_6472+17dup
XM_024453287.1:c.5137+1_5137+17dup
NM_000573.4:c.5122+1_5122+17dup
NM_000651.6:c.6472+1_6472+17dup