Canonical Allele Identifier: CA2650268355
Gene: CR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207580182G>T , CM000663.2:g.207580182G>T GRCh38
NC_000001.10:g.207753527G>T , CM000663.1:g.207753527G>T GRCh37
NC_000001.9:g.205820150G>T NCBI36
NG_007481.1:g.89055G>T

Transcript Alleles

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