Canonical Allele Identifier: CA344545241
Gene: CR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.207611827G>C , CM000663.2:g.207611827G>C GRCh38
NC_000001.10:g.207785172G>C , CM000663.1:g.207785172G>C GRCh37
NC_000001.9:g.205851795G>C NCBI36
NG_007481.1:g.120700G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367049.9:c.6446G>C MANE Select ENSP00000356016.4:p.Trp2149Ser
ENST00000367051.6:c.5096G>C ENSP00000356018.1:p.Trp1699Ser
ENST00000367052.6:c.5096G>C ENSP00000356019.1:p.Trp1699Ser
ENST00000367053.6:c.5096G>C ENSP00000356020.1:p.Trp1699Ser
ENST00000400960.7:c.5096G>C ENSP00000383744.2:p.Trp1699Ser
ENST00000367049.8:c.6446G>C ENSP00000356016.4:p.Trp2149Ser
ENST00000367051.5:c.5096G>C ENSP00000356018.1:p.Trp1699Ser
ENST00000367052.5:c.5096G>C ENSP00000356019.1:p.Trp1699Ser
ENST00000367053.5:c.5096G>C ENSP00000356020.1:p.Trp1699Ser
ENST00000400960.6:c.5096G>C ENSP00000383744.2:p.Trp1699Ser
ENST00000529814.1:c.1180-4748G>C
NM_000573.3:c.5096G>C NP_000564.2:p.Trp1699Ser
NM_000651.4:c.6446G>C NP_000642.3:p.Trp2149Ser
XM_006711166.2:c.6461G>C XP_006711229.1:p.Trp2154Ser
XM_011509205.1:c.6461G>C XP_011507507.1:p.Trp2154Ser
NM_000651.5:c.6446G>C NP_000642.3:p.Trp2149Ser
XM_024453287.1:c.5111G>C XP_024309055.1:p.Trp1704Ser
NM_000573.4:c.5096G>C NP_000564.2:p.Trp1699Ser
NM_000651.6:c.6446G>C MANE Select NP_000642.3:p.Trp2149Ser