Canonical Allele Identifier: CA2483456586
Gene: CR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207611852_207611869delinsAGGTGCCTTGACTCTCTG , CM000663.2:g.207611852_207611869delinsAGGTGCCTTGACTCTCTG GRCh38
NC_000001.10:g.207785197_207785214delinsAGGTGCCTTGACTCTCTG , CM000663.1:g.207785197_207785214delinsAGGTGCCTTGACTCTCTG GRCh37
NC_000001.9:g.205851820_205851837delinsAGGTGCCTTGACTCTCTG NCBI36
NG_007481.1:g.120725_120742delinsAGGTGCCTTGACTCTCTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000367049.9:c.6471_6472+16delinsAGGTGCCTTGACTCTCTG
ENST00000367051.6:c.5121_5122+16delinsAGGTGCCTTGACTCTCTG
ENST00000367052.6:c.5121_5122+16delinsAGGTGCCTTGACTCTCTG
ENST00000367053.6:c.5121_5122+16delinsAGGTGCCTTGACTCTCTG
ENST00000400960.7:c.5121_5122+16delinsAGGTGCCTTGACTCTCTG
ENST00000367049.8:c.6471_6472+16delinsAGGTGCCTTGACTCTCTG
ENST00000367051.5:c.5121_5122+16delinsAGGTGCCTTGACTCTCTG
ENST00000367052.5:c.5121_5122+16delinsAGGTGCCTTGACTCTCTG
ENST00000367053.5:c.5121_5122+16delinsAGGTGCCTTGACTCTCTG
ENST00000400960.6:c.5121_5122+16delinsAGGTGCCTTGACTCTCTG
ENST00000529814.1:c.1180-4723_1180-4706delinsAGGTGCCTTGACTCTCTG
NM_000573.3:c.5121_5122+16delinsAGGTGCCTTGACTCTCTG
NM_000651.4:c.6471_6472+16delinsAGGTGCCTTGACTCTCTG
XM_006711166.2:c.6486_6487+16delinsAGGTGCCTTGACTCTCTG
XM_011509205.1:c.6486_6487+16delinsAGGTGCCTTGACTCTCTG
NM_000651.5:c.6471_6472+16delinsAGGTGCCTTGACTCTCTG
XM_024453287.1:c.5136_5137+16delinsAGGTGCCTTGACTCTCTG
NM_000573.4:c.5121_5122+16delinsAGGTGCCTTGACTCTCTG
NM_000651.6:c.6471_6472+16delinsAGGTGCCTTGACTCTCTG