Canonical Allele Identifier: CA2483443619
Gene: CR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207580175_207580176delinsGT , CM000663.2:g.207580175_207580176delinsGT GRCh38
NC_000001.10:g.207753520_207753521delinsGT , CM000663.1:g.207753520_207753521delinsGT GRCh37
NC_000001.9:g.205820143_205820144delinsGT NCBI36
NG_007481.1:g.89048_89049delinsGT

Transcript Alleles

HGVS Amino-acid change
ENST00000367049.9:c.4937-65_4937-64delinsGT MANE Select ENSP00000356016.4:n.4937-65_4937-64delins...
ENST00000367051.6:c.3587-65_3587-64delinsGT ENSP00000356018.1:n.3587-65_3587-64delins...
ENST00000367052.6:c.3587-65_3587-64delinsGT ENSP00000356019.1:n.3587-65_3587-64delins...
ENST00000367053.6:c.3587-65_3587-64delinsGT ENSP00000356020.1:n.3587-65_3587-64delins...
ENST00000400960.7:c.3587-65_3587-64delinsGT ENSP00000383744.2:n.3587-65_3587-64delins...
ENST00000367049.8:c.4937-65_4937-64delinsGT ENSP00000356016.4:n.4937-65_4937-64delins...
ENST00000367051.5:c.3587-65_3587-64delinsGT ENSP00000356018.1:n.3587-65_3587-64delins...
ENST00000367052.5:c.3587-65_3587-64delinsGT ENSP00000356019.1:n.3587-65_3587-64delins...
ENST00000367053.5:c.3587-65_3587-64delinsGT ENSP00000356020.1:n.3587-65_3587-64delins...
ENST00000400960.6:c.3587-65_3587-64delinsGT ENSP00000383744.2:n.3587-65_3587-64delins...
ENST00000529814.1:c.1179+14252_1179+14253delinsGT
ENST00000534202.5:c.*702-65_*702-64delinsGT ENSP00000436139.2:n.*702-65_*702-64delins...
NM_000573.3:c.3587-65_3587-64delinsGT NP_000564.2:n.3587-65_3587-64delinsGT
NM_000651.4:c.4937-65_4937-64delinsGT NP_000642.3:n.4937-65_4937-64delinsGT
XM_006711166.2:c.4952-65_4952-64delinsGT XP_006711229.1:n.4952-65_4952-64delinsGT
XM_011509205.1:c.4952-65_4952-64delinsGT XP_011507507.1:n.4952-65_4952-64delinsGT
NM_000651.5:c.4937-65_4937-64delinsGT NP_000642.3:n.4937-65_4937-64delinsGT
XM_024453287.1:c.3602-65_3602-64delinsGT XP_024309055.1:n.3602-65_3602-64delinsGT
NM_000573.4:c.3587-65_3587-64delinsGT NP_000564.2:n.3587-65_3587-64delinsGT
NM_000651.6:c.4937-65_4937-64delinsGT MANE Select NP_000642.3:n.4937-65_4937-64delinsGT