Canonical Allele Identifier: CA344545186

Gene: CR1

Linked Data

• MyVariant Identifiers: chr1:g.207785147C>G (hg19) ; chr1:g.207611802C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207611802C>G , CM000663.2:g.207611802C>G	GRCh38
NC_000001.10:g.207785147C>G , CM000663.1:g.207785147C>G	GRCh37
NC_000001.9:g.205851770C>G	NCBI36
NG_007481.1:g.120675C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367049.9:c.6421C>G MANE Select	ENSP00000356016.4:p.Leu2141Val
ENST00000367051.6:c.5071C>G	ENSP00000356018.1:p.Leu1691Val
ENST00000367052.6:c.5071C>G	ENSP00000356019.1:p.Leu1691Val
ENST00000367053.6:c.5071C>G	ENSP00000356020.1:p.Leu1691Val
ENST00000400960.7:c.5071C>G	ENSP00000383744.2:p.Leu1691Val
ENST00000367049.8:c.6421C>G	ENSP00000356016.4:p.Leu2141Val
ENST00000367051.5:c.5071C>G	ENSP00000356018.1:p.Leu1691Val
ENST00000367052.5:c.5071C>G	ENSP00000356019.1:p.Leu1691Val
ENST00000367053.5:c.5071C>G	ENSP00000356020.1:p.Leu1691Val
ENST00000400960.6:c.5071C>G	ENSP00000383744.2:p.Leu1691Val
ENST00000529814.1:c.1180-4773C>G
NM_000573.3:c.5071C>G	NP_000564.2:p.Leu1691Val
NM_000651.4:c.6421C>G	NP_000642.3:p.Leu2141Val
XM_006711166.2:c.6436C>G	XP_006711229.1:p.Leu2146Val
XM_011509205.1:c.6436C>G	XP_011507507.1:p.Leu2146Val
NM_000651.5:c.6421C>G	NP_000642.3:p.Leu2141Val
XM_024453287.1:c.5086C>G	XP_024309055.1:p.Leu1696Val
NM_000573.4:c.5071C>G	NP_000564.2:p.Leu1691Val
NM_000651.6:c.6421C>G MANE Select	NP_000642.3:p.Leu2141Val