Canonical Allele Identifier: CA344545126

Gene: CR1

Linked Data

• MyVariant Identifiers: chr1:g.207785117C>A (hg19) ; chr1:g.207611772C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207611772C>A , CM000663.2:g.207611772C>A	GRCh38
NC_000001.10:g.207785117C>A , CM000663.1:g.207785117C>A	GRCh37
NC_000001.9:g.205851740C>A	NCBI36
NG_007481.1:g.120645C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367049.9:c.6391C>A MANE Select	ENSP00000356016.4:p.Pro2131Thr
ENST00000367051.6:c.5041C>A	ENSP00000356018.1:p.Pro1681Thr
ENST00000367052.6:c.5041C>A	ENSP00000356019.1:p.Pro1681Thr
ENST00000367053.6:c.5041C>A	ENSP00000356020.1:p.Pro1681Thr
ENST00000400960.7:c.5041C>A	ENSP00000383744.2:p.Pro1681Thr
ENST00000367049.8:c.6391C>A	ENSP00000356016.4:p.Pro2131Thr
ENST00000367051.5:c.5041C>A	ENSP00000356018.1:p.Pro1681Thr
ENST00000367052.5:c.5041C>A	ENSP00000356019.1:p.Pro1681Thr
ENST00000367053.5:c.5041C>A	ENSP00000356020.1:p.Pro1681Thr
ENST00000400960.6:c.5041C>A	ENSP00000383744.2:p.Pro1681Thr
ENST00000529814.1:c.1180-4803C>A
NM_000573.3:c.5041C>A	NP_000564.2:p.Pro1681Thr
NM_000651.4:c.6391C>A	NP_000642.3:p.Pro2131Thr
XM_006711166.2:c.6406C>A	XP_006711229.1:p.Pro2136Thr
XM_011509205.1:c.6406C>A	XP_011507507.1:p.Pro2136Thr
NM_000651.5:c.6391C>A	NP_000642.3:p.Pro2131Thr
XM_024453287.1:c.5056C>A	XP_024309055.1:p.Pro1686Thr
NM_000573.4:c.5041C>A	NP_000564.2:p.Pro1681Thr
NM_000651.6:c.6391C>A MANE Select	NP_000642.3:p.Pro2131Thr