Canonical Allele Identifier: CA344545000

Gene: CR1

Linked Data

• gnomAD v4: 1-207611716-C-A
• MyVariant Identifiers: chr1:g.207785061C>A (hg19) ; chr1:g.207611716C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207611716C>A , CM000663.2:g.207611716C>A	GRCh38
NC_000001.10:g.207785061C>A , CM000663.1:g.207785061C>A	GRCh37
NC_000001.9:g.205851684C>A	NCBI36
NG_007481.1:g.120589C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367049.9:c.6335C>A MANE Select	ENSP00000356016.4:p.Thr2112Asn
ENST00000367051.6:c.4985C>A	ENSP00000356018.1:p.Thr1662Asn
ENST00000367052.6:c.4985C>A	ENSP00000356019.1:p.Thr1662Asn
ENST00000367053.6:c.4985C>A	ENSP00000356020.1:p.Thr1662Asn
ENST00000400960.7:c.4985C>A	ENSP00000383744.2:p.Thr1662Asn
ENST00000367049.8:c.6335C>A	ENSP00000356016.4:p.Thr2112Asn
ENST00000367051.5:c.4985C>A	ENSP00000356018.1:p.Thr1662Asn
ENST00000367052.5:c.4985C>A	ENSP00000356019.1:p.Thr1662Asn
ENST00000367053.5:c.4985C>A	ENSP00000356020.1:p.Thr1662Asn
ENST00000400960.6:c.4985C>A	ENSP00000383744.2:p.Thr1662Asn
ENST00000529814.1:c.1180-4859C>A
NM_000573.3:c.4985C>A	NP_000564.2:p.Thr1662Asn
NM_000651.4:c.6335C>A	NP_000642.3:p.Thr2112Asn
XM_006711166.2:c.6350C>A	XP_006711229.1:p.Thr2117Asn
XM_011509205.1:c.6350C>A	XP_011507507.1:p.Thr2117Asn
NM_000651.5:c.6335C>A	NP_000642.3:p.Thr2112Asn
XM_024453287.1:c.5000C>A	XP_024309055.1:p.Thr1667Asn
NM_000573.4:c.4985C>A	NP_000564.2:p.Thr1662Asn
NM_000651.6:c.6335C>A MANE Select	NP_000642.3:p.Thr2112Asn