Canonical Allele Identifier: CA1369431

Gene: CR1

Linked Data

• dbSNP Id: rs752545769
• ExAC: 1:207696907 A / T
• gnomAD v2: 1-207696907-A-T
• gnomAD v4: 1-207523562-A-T
• MyVariant Identifiers: chr1:g.207696907A>T (hg19) ; chr1:g.207523562A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207523562A>T , CM000663.2:g.207523562A>T	GRCh38
NC_000001.10:g.207696907A>T , CM000663.1:g.207696907A>T	GRCh37
NC_000001.9:g.205763530A>T	NCBI36
NG_007481.1:g.32435A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000367049.9:c.488-49A>T MANE Select	ENSP00000356016.4:n.488-49A>T
ENST00000367051.6:c.487+11908A>T	ENSP00000356018.1:n.487+11908A>T
ENST00000367052.6:c.488-49A>T	ENSP00000356019.1:n.488-49A>T
ENST00000367053.6:c.488-49A>T	ENSP00000356020.1:n.488-49A>T
ENST00000400960.7:c.488-49A>T	ENSP00000383744.2:n.488-49A>T
ENST00000367049.8:c.488-49A>T	ENSP00000356016.4:n.488-49A>T
ENST00000367050.8:n.609-49A>T
ENST00000367051.5:c.487+11908A>T	ENSP00000356018.1:n.487+11908A>T
ENST00000367052.5:c.488-49A>T	ENSP00000356019.1:n.488-49A>T
ENST00000367053.5:c.488-49A>T	ENSP00000356020.1:n.488-49A>T
ENST00000400960.6:c.488-49A>T	ENSP00000383744.2:n.488-49A>T
ENST00000434033.5:n.415-49A>T
ENST00000436595.1:n.414+11908A>T
ENST00000450439.5:n.415-49A>T
ENST00000529814.1:c.415-49A>T
ENST00000534202.5:c.488-49A>T	ENSP00000436139.2:n.488-49A>T
NM_000573.3:c.488-49A>T	NP_000564.2:n.488-49A>T
NM_000651.4:c.488-49A>T	NP_000642.3:n.488-49A>T
XM_006711166.2:c.503-49A>T	XP_006711229.1:n.503-49A>T
XM_011509205.1:c.503-49A>T	XP_011507507.1:n.503-49A>T
NM_000651.5:c.488-49A>T	NP_000642.3:n.488-49A>T
XM_024453287.1:c.503-49A>T	XP_024309055.1:n.503-49A>T
NM_000573.4:c.488-49A>T	NP_000564.2:n.488-49A>T
NM_000651.6:c.488-49A>T MANE Select	NP_000642.3:n.488-49A>T