Canonical Allele Identifier: CA2483456452
Gene: CR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207611506_207611507delinsCT , CM000663.2:g.207611506_207611507delinsCT GRCh38
NC_000001.10:g.207784851_207784852delinsCT , CM000663.1:g.207784851_207784852delinsCT GRCh37
NC_000001.9:g.205851474_205851475delinsCT NCBI36
NG_007481.1:g.120379_120380delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000367049.9:c.6296-171_6296-170delinsCT MANE Select ENSP00000356016.4:n.6296-171_6296-170delinsCT
ENST00000367051.6:c.4946-171_4946-170delinsCT ENSP00000356018.1:n.4946-171_4946-170delinsCT
ENST00000367052.6:c.4946-171_4946-170delinsCT ENSP00000356019.1:n.4946-171_4946-170delinsCT
ENST00000367053.6:c.4946-171_4946-170delinsCT ENSP00000356020.1:n.4946-171_4946-170delinsCT
ENST00000400960.7:c.4946-171_4946-170delinsCT ENSP00000383744.2:n.4946-171_4946-170delinsCT
ENST00000367049.8:c.6296-171_6296-170delinsCT ENSP00000356016.4:n.6296-171_6296-170delinsCT
ENST00000367051.5:c.4946-171_4946-170delinsCT ENSP00000356018.1:n.4946-171_4946-170delinsCT
ENST00000367052.5:c.4946-171_4946-170delinsCT ENSP00000356019.1:n.4946-171_4946-170delinsCT
ENST00000367053.5:c.4946-171_4946-170delinsCT ENSP00000356020.1:n.4946-171_4946-170delinsCT
ENST00000400960.6:c.4946-171_4946-170delinsCT ENSP00000383744.2:n.4946-171_4946-170delinsCT
ENST00000529814.1:c.1180-5069_1180-5068delinsCT
NM_000573.3:c.4946-171_4946-170delinsCT NP_000564.2:n.4946-171_4946-170delinsCT
NM_000651.4:c.6296-171_6296-170delinsCT NP_000642.3:n.6296-171_6296-170delinsCT
XM_006711166.2:c.6311-171_6311-170delinsCT XP_006711229.1:n.6311-171_6311-170delinsCT
XM_011509205.1:c.6311-171_6311-170delinsCT XP_011507507.1:n.6311-171_6311-170delinsCT
NM_000651.5:c.6296-171_6296-170delinsCT NP_000642.3:n.6296-171_6296-170delinsCT
XM_024453287.1:c.4961-171_4961-170delinsCT XP_024309055.1:n.4961-171_4961-170delinsCT
NM_000573.4:c.4946-171_4946-170delinsCT NP_000564.2:n.4946-171_4946-170delinsCT
NM_000651.6:c.6296-171_6296-170delinsCT MANE Select NP_000642.3:n.6296-171_6296-170delinsCT