Canonical Allele Identifier: CA2483445420
Gene: CR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207584210T= , CM000663.2:g.207584210T= GRCh38
NC_000001.10:g.207757555T= , CM000663.1:g.207757555T= GRCh37
NC_000001.9:g.205824178T= NCBI36
NG_007481.1:g.93083T=

Transcript Alleles

HGVS Amino-acid change
ENST00000367049.9:c.5303-439T= MANE Select ENSP00000356016.4:n.5303-439T=
ENST00000367051.6:c.3953-439T= ENSP00000356018.1:n.3953-439T=
ENST00000367052.6:c.3953-439T= ENSP00000356019.1:n.3953-439T=
ENST00000367053.6:c.3953-439T= ENSP00000356020.1:n.3953-439T=
ENST00000400960.7:c.3953-439T= ENSP00000383744.2:n.3953-439T=
ENST00000367049.8:c.5303-439T= ENSP00000356016.4:n.5303-439T=
ENST00000367051.5:c.3953-439T= ENSP00000356018.1:n.3953-439T=
ENST00000367052.5:c.3953-439T= ENSP00000356019.1:n.3953-439T=
ENST00000367053.5:c.3953-439T= ENSP00000356020.1:n.3953-439T=
ENST00000400960.6:c.3953-439T= ENSP00000383744.2:n.3953-439T=
ENST00000529814.1:c.1179+18287T=
ENST00000534202.5:c.*1068-439T= ENSP00000436139.2:n.*1068-439T=
NM_000573.3:c.3953-439T= NP_000564.2:n.3953-439T=
NM_000651.4:c.5303-439T= NP_000642.3:n.5303-439T=
XM_006711166.2:c.5318-439T= XP_006711229.1:n.5318-439T=
XM_011509205.1:c.5318-439T= XP_011507507.1:n.5318-439T=
NM_000651.5:c.5303-439T= NP_000642.3:n.5303-439T=
XM_024453287.1:c.3968-439T= XP_024309055.1:n.3968-439T=
NM_000573.4:c.3953-439T= NP_000564.2:n.3953-439T=
NM_000651.6:c.5303-439T= MANE Select NP_000642.3:n.5303-439T=