Canonical Allele Identifier: CA344545131

Gene: CR1

Linked Data

• MyVariant Identifiers: chr1:g.207785118C>T (hg19) ; chr1:g.207611773C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207611773C>T , CM000663.2:g.207611773C>T	GRCh38
NC_000001.10:g.207785118C>T , CM000663.1:g.207785118C>T	GRCh37
NC_000001.9:g.205851741C>T	NCBI36
NG_007481.1:g.120646C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367049.9:c.6392C>T MANE Select	ENSP00000356016.4:p.Pro2131Leu
ENST00000367051.6:c.5042C>T	ENSP00000356018.1:p.Pro1681Leu
ENST00000367052.6:c.5042C>T	ENSP00000356019.1:p.Pro1681Leu
ENST00000367053.6:c.5042C>T	ENSP00000356020.1:p.Pro1681Leu
ENST00000400960.7:c.5042C>T	ENSP00000383744.2:p.Pro1681Leu
ENST00000367049.8:c.6392C>T	ENSP00000356016.4:p.Pro2131Leu
ENST00000367051.5:c.5042C>T	ENSP00000356018.1:p.Pro1681Leu
ENST00000367052.5:c.5042C>T	ENSP00000356019.1:p.Pro1681Leu
ENST00000367053.5:c.5042C>T	ENSP00000356020.1:p.Pro1681Leu
ENST00000400960.6:c.5042C>T	ENSP00000383744.2:p.Pro1681Leu
ENST00000529814.1:c.1180-4802C>T
NM_000573.3:c.5042C>T	NP_000564.2:p.Pro1681Leu
NM_000651.4:c.6392C>T	NP_000642.3:p.Pro2131Leu
XM_006711166.2:c.6407C>T	XP_006711229.1:p.Pro2136Leu
XM_011509205.1:c.6407C>T	XP_011507507.1:p.Pro2136Leu
NM_000651.5:c.6392C>T	NP_000642.3:p.Pro2131Leu
XM_024453287.1:c.5057C>T	XP_024309055.1:p.Pro1686Leu
NM_000573.4:c.5042C>T	NP_000564.2:p.Pro1681Leu
NM_000651.6:c.6392C>T MANE Select	NP_000642.3:p.Pro2131Leu