Canonical Allele Identifier: CA1369460
Gene: CR1 HGNC NCBI

Linked Data

dbSNP Id: rs758794007

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207523682T>G , CM000663.2:g.207523682T>G GRCh38
NC_000001.10:g.207697027T>G , CM000663.1:g.207697027T>G GRCh37
NC_000001.9:g.205763650T>G NCBI36
NG_007481.1:g.32555T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367049.9:c.559T>G MANE Select ENSP00000356016.4:p.Tyr187Asp
ENST00000367051.6:c.487+12028T>G ENSP00000356018.1:n.487+12028T>G
ENST00000367052.6:c.559T>G ENSP00000356019.1:p.Tyr187Asp
ENST00000367053.6:c.559T>G ENSP00000356020.1:p.Tyr187Asp
ENST00000400960.7:c.559T>G ENSP00000383744.2:p.Tyr187Asp
ENST00000367049.8:c.559T>G ENSP00000356016.4:p.Tyr187Asp
ENST00000367050.8:n.680T>G
ENST00000367051.5:c.487+12028T>G ENSP00000356018.1:n.487+12028T>G
ENST00000367052.5:c.559T>G ENSP00000356019.1:p.Tyr187Asp
ENST00000367053.5:c.559T>G ENSP00000356020.1:p.Tyr187Asp
ENST00000400960.6:c.559T>G ENSP00000383744.2:p.Tyr187Asp
ENST00000434033.5:n.486T>G
ENST00000436595.1:n.414+12028T>G
ENST00000450439.5:n.486T>G
ENST00000529814.1:c.486T>G
ENST00000534202.5:c.559T>G ENSP00000436139.2:p.Tyr187Asp
NM_000573.3:c.559T>G NP_000564.2:p.Tyr187Asp
NM_000651.4:c.559T>G NP_000642.3:p.Tyr187Asp
XM_006711166.2:c.574T>G XP_006711229.1:p.Tyr192Asp
XM_011509205.1:c.574T>G XP_011507507.1:p.Tyr192Asp
NM_000651.5:c.559T>G NP_000642.3:p.Tyr187Asp
XM_024453287.1:c.574T>G XP_024309055.1:p.Tyr192Asp
NM_000573.4:c.559T>G NP_000564.2:p.Tyr187Asp
NM_000651.6:c.559T>G MANE Select NP_000642.3:p.Tyr187Asp