Canonical Allele Identifier: CA344520569

Gene: CR1

Linked Data

• dbSNP Id: rs1660074264
• gnomAD v4: 1-207523790-G-A
• MyVariant Identifiers: chr1:g.207697135G>A (hg19) ; chr1:g.207523790G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207523790G>A , CM000663.2:g.207523790G>A	GRCh38
NC_000001.10:g.207697135G>A , CM000663.1:g.207697135G>A	GRCh37
NC_000001.9:g.205763758G>A	NCBI36
NG_007481.1:g.32663G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367049.9:c.667G>A MANE Select	ENSP00000356016.4:p.Gly223Ser
ENST00000367051.6:c.487+12136G>A	ENSP00000356018.1:n.487+12136G>A
ENST00000367052.6:c.667G>A	ENSP00000356019.1:p.Gly223Ser
ENST00000367053.6:c.667G>A	ENSP00000356020.1:p.Gly223Ser
ENST00000400960.7:c.667G>A	ENSP00000383744.2:p.Gly223Ser
ENST00000367049.8:c.667G>A	ENSP00000356016.4:p.Gly223Ser
ENST00000367050.8:n.788G>A
ENST00000367051.5:c.487+12136G>A	ENSP00000356018.1:n.487+12136G>A
ENST00000367052.5:c.667G>A	ENSP00000356019.1:p.Gly223Ser
ENST00000367053.5:c.667G>A	ENSP00000356020.1:p.Gly223Ser
ENST00000400960.6:c.667G>A	ENSP00000383744.2:p.Gly223Ser
ENST00000434033.5:n.594G>A
ENST00000436595.1:n.414+12136G>A
ENST00000450439.5:n.594G>A
ENST00000529814.1:c.594G>A
ENST00000534202.5:c.667G>A	ENSP00000436139.2:p.Gly223Ser
NM_000573.3:c.667G>A	NP_000564.2:p.Gly223Ser
NM_000651.4:c.667G>A	NP_000642.3:p.Gly223Ser
XM_006711166.2:c.682G>A	XP_006711229.1:p.Gly228Ser
XM_011509205.1:c.682G>A	XP_011507507.1:p.Gly228Ser
NM_000651.5:c.667G>A	NP_000642.3:p.Gly223Ser
XM_024453287.1:c.682G>A	XP_024309055.1:p.Gly228Ser
NM_000573.4:c.667G>A	NP_000564.2:p.Gly223Ser
NM_000651.6:c.667G>A MANE Select	NP_000642.3:p.Gly223Ser