Canonical Allele Identifier: CA1145321198
Gene: CR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207611853_207611870delinsGGTGCCTTGACTCTCTGG , CM000663.2:g.207611853_207611870delinsGGTGCCTTGACTCTCTGG GRCh38
NC_000001.10:g.207785198_207785215delinsGGTGCCTTGACTCTCTGG , CM000663.1:g.207785198_207785215delinsGGTGCCTTGACTCTCTGG GRCh37
NC_000001.9:g.205851821_205851838delinsGGTGCCTTGACTCTCTGG NCBI36
NG_007481.1:g.120726_120743delinsGGTGCCTTGACTCTCTGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000367049.9:c.6472_6472+17delinsGGTGCCTTGACTCTCTGG
ENST00000367051.6:c.5122_5122+17delinsGGTGCCTTGACTCTCTGG
ENST00000367052.6:c.5122_5122+17delinsGGTGCCTTGACTCTCTGG
ENST00000367053.6:c.5122_5122+17delinsGGTGCCTTGACTCTCTGG
ENST00000400960.7:c.5122_5122+17delinsGGTGCCTTGACTCTCTGG
ENST00000367049.8:c.6472_6472+17delinsGGTGCCTTGACTCTCTGG
ENST00000367051.5:c.5122_5122+17delinsGGTGCCTTGACTCTCTGG
ENST00000367052.5:c.5122_5122+17delinsGGTGCCTTGACTCTCTGG
ENST00000367053.5:c.5122_5122+17delinsGGTGCCTTGACTCTCTGG
ENST00000400960.6:c.5122_5122+17delinsGGTGCCTTGACTCTCTGG
ENST00000529814.1:c.1180-4722_1180-4705delinsGGTGCCTTGACTCTCTGG
NM_000573.3:c.5122_5122+17delinsGGTGCCTTGACTCTCTGG
NM_000651.4:c.6472_6472+17delinsGGTGCCTTGACTCTCTGG
XM_006711166.2:c.6487_6487+17delinsGGTGCCTTGACTCTCTGG
XM_011509205.1:c.6487_6487+17delinsGGTGCCTTGACTCTCTGG
NM_000651.5:c.6472_6472+17delinsGGTGCCTTGACTCTCTGG
XM_024453287.1:c.5137_5137+17delinsGGTGCCTTGACTCTCTGG
NM_000573.4:c.5122_5122+17delinsGGTGCCTTGACTCTCTGG
NM_000651.6:c.6472_6472+17delinsGGTGCCTTGACTCTCTGG