Canonical Allele Identifier: CA1011643798
Gene: CR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207584196_207584199del , CM000663.2:g.207584196_207584199del GRCh38
NC_000001.10:g.207757541_207757544del , CM000663.1:g.207757541_207757544del GRCh37
NC_000001.9:g.205824164_205824167del NCBI36
NG_007481.1:g.93069_93072del

Transcript Alleles

HGVS Amino-acid Change
ENST00000367049.9:c.5303-453_5303-450del MANE Select ENSP00000356016.4:n.5303-453_5303-450del
ENST00000367051.6:c.3953-453_3953-450del ENSP00000356018.1:n.3953-453_3953-450del
ENST00000367052.6:c.3953-453_3953-450del ENSP00000356019.1:n.3953-453_3953-450del
ENST00000367053.6:c.3953-453_3953-450del ENSP00000356020.1:n.3953-453_3953-450del
ENST00000400960.7:c.3953-453_3953-450del ENSP00000383744.2:n.3953-453_3953-450del
ENST00000367049.8:c.5303-453_5303-450del ENSP00000356016.4:n.5303-453_5303-450del
ENST00000367051.5:c.3953-453_3953-450del ENSP00000356018.1:n.3953-453_3953-450del
ENST00000367052.5:c.3953-453_3953-450del ENSP00000356019.1:n.3953-453_3953-450del
ENST00000367053.5:c.3953-453_3953-450del ENSP00000356020.1:n.3953-453_3953-450del
ENST00000400960.6:c.3953-453_3953-450del ENSP00000383744.2:n.3953-453_3953-450del
ENST00000529814.1:c.1179+18273_1179+18276del
ENST00000534202.5:c.*1068-453_*1068-450del ENSP00000436139.2:n.*1068-453_*1068-450del
NM_000573.3:c.3953-453_3953-450del NP_000564.2:n.3953-453_3953-450del
NM_000651.4:c.5303-453_5303-450del NP_000642.3:n.5303-453_5303-450del
XM_006711166.2:c.5318-453_5318-450del XP_006711229.1:n.5318-453_5318-450del
XM_011509205.1:c.5318-453_5318-450del XP_011507507.1:n.5318-453_5318-450del
NM_000651.5:c.5303-453_5303-450del NP_000642.3:n.5303-453_5303-450del
XM_024453287.1:c.3968-453_3968-450del XP_024309055.1:n.3968-453_3968-450del
NM_000573.4:c.3953-453_3953-450del NP_000564.2:n.3953-453_3953-450del
NM_000651.6:c.5303-453_5303-450del MANE Select NP_000642.3:n.5303-453_5303-450del