Canonical Allele Identifier: CA2483443620
Gene: CR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207580181_207580182delinsAG , CM000663.2:g.207580181_207580182delinsAG GRCh38
NC_000001.10:g.207753526_207753527delinsAG , CM000663.1:g.207753526_207753527delinsAG GRCh37
NC_000001.9:g.205820149_205820150delinsAG NCBI36
NG_007481.1:g.89054_89055delinsAG

Transcript Alleles

HGVS Amino-acid change
ENST00000367049.9:c.4937-59_4937-58delinsAG MANE Select ENSP00000356016.4:n.4937-59_4937-58delins...
ENST00000367051.6:c.3587-59_3587-58delinsAG ENSP00000356018.1:n.3587-59_3587-58delins...
ENST00000367052.6:c.3587-59_3587-58delinsAG ENSP00000356019.1:n.3587-59_3587-58delins...
ENST00000367053.6:c.3587-59_3587-58delinsAG ENSP00000356020.1:n.3587-59_3587-58delins...
ENST00000400960.7:c.3587-59_3587-58delinsAG ENSP00000383744.2:n.3587-59_3587-58delins...
ENST00000367049.8:c.4937-59_4937-58delinsAG ENSP00000356016.4:n.4937-59_4937-58delins...
ENST00000367051.5:c.3587-59_3587-58delinsAG ENSP00000356018.1:n.3587-59_3587-58delins...
ENST00000367052.5:c.3587-59_3587-58delinsAG ENSP00000356019.1:n.3587-59_3587-58delins...
ENST00000367053.5:c.3587-59_3587-58delinsAG ENSP00000356020.1:n.3587-59_3587-58delins...
ENST00000400960.6:c.3587-59_3587-58delinsAG ENSP00000383744.2:n.3587-59_3587-58delins...
ENST00000529814.1:c.1179+14258_1179+14259delinsAG
ENST00000534202.5:c.*702-59_*702-58delinsAG ENSP00000436139.2:n.*702-59_*702-58delins...
NM_000573.3:c.3587-59_3587-58delinsAG NP_000564.2:n.3587-59_3587-58delinsAG
NM_000651.4:c.4937-59_4937-58delinsAG NP_000642.3:n.4937-59_4937-58delinsAG
XM_006711166.2:c.4952-59_4952-58delinsAG XP_006711229.1:n.4952-59_4952-58delinsAG
XM_011509205.1:c.4952-59_4952-58delinsAG XP_011507507.1:n.4952-59_4952-58delinsAG
NM_000651.5:c.4937-59_4937-58delinsAG NP_000642.3:n.4937-59_4937-58delinsAG
XM_024453287.1:c.3602-59_3602-58delinsAG XP_024309055.1:n.3602-59_3602-58delinsAG
NM_000573.4:c.3587-59_3587-58delinsAG NP_000564.2:n.3587-59_3587-58delinsAG
NM_000651.6:c.4937-59_4937-58delinsAG MANE Select NP_000642.3:n.4937-59_4937-58delinsAG