Canonical Allele Identifier: CA2650268356
Gene: CR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207580183G>A , CM000663.2:g.207580183G>A GRCh38
NC_000001.10:g.207753528G>A , CM000663.1:g.207753528G>A GRCh37
NC_000001.9:g.205820151G>A NCBI36
NG_007481.1:g.89056G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000367049.9:c.4937-57G>A MANE Select ENSP00000356016.4:n.4937-57G>A
ENST00000367051.6:c.3587-57G>A ENSP00000356018.1:n.3587-57G>A
ENST00000367052.6:c.3587-57G>A ENSP00000356019.1:n.3587-57G>A
ENST00000367053.6:c.3587-57G>A ENSP00000356020.1:n.3587-57G>A
ENST00000400960.7:c.3587-57G>A ENSP00000383744.2:n.3587-57G>A
ENST00000367049.8:c.4937-57G>A ENSP00000356016.4:n.4937-57G>A
ENST00000367051.5:c.3587-57G>A ENSP00000356018.1:n.3587-57G>A
ENST00000367052.5:c.3587-57G>A ENSP00000356019.1:n.3587-57G>A
ENST00000367053.5:c.3587-57G>A ENSP00000356020.1:n.3587-57G>A
ENST00000400960.6:c.3587-57G>A ENSP00000383744.2:n.3587-57G>A
ENST00000529814.1:c.1179+14260G>A
ENST00000534202.5:c.*702-57G>A ENSP00000436139.2:n.*702-57G>A
NM_000573.3:c.3587-57G>A NP_000564.2:n.3587-57G>A
NM_000651.4:c.4937-57G>A NP_000642.3:n.4937-57G>A
XM_006711166.2:c.4952-57G>A XP_006711229.1:n.4952-57G>A
XM_011509205.1:c.4952-57G>A XP_011507507.1:n.4952-57G>A
NM_000651.5:c.4937-57G>A NP_000642.3:n.4937-57G>A
XM_024453287.1:c.3602-57G>A XP_024309055.1:n.3602-57G>A
NM_000573.4:c.3587-57G>A NP_000564.2:n.3587-57G>A
NM_000651.6:c.4937-57G>A MANE Select NP_000642.3:n.4937-57G>A