Canonical Allele Identifier: CA422957742

Gene: CR1

Linked Data

• MyVariant Identifiers: chr1:g.207697254G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207523909G>T , CM000663.2:g.207523909G>T	GRCh38
NC_000001.10:g.207697254G>T , CM000663.1:g.207697254G>T	GRCh37
NC_000001.9:g.205763877G>T	NCBI36
NG_007481.1:g.32782G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367049.9:c.786G>T MANE Select	ENSP00000356016.4:p.Val262=
ENST00000367051.6:c.487+12255G>T	ENSP00000356018.1:n.487+12255G>T
ENST00000367052.6:c.786G>T	ENSP00000356019.1:p.Val262=
ENST00000367053.6:c.786G>T	ENSP00000356020.1:p.Val262=
ENST00000400960.7:c.786G>T	ENSP00000383744.2:p.Val262=
ENST00000367049.8:c.786G>T	ENSP00000356016.4:p.Val262=
ENST00000367050.8:n.907G>T
ENST00000367051.5:c.487+12255G>T	ENSP00000356018.1:n.487+12255G>T
ENST00000367052.5:c.786G>T	ENSP00000356019.1:p.Val262=
ENST00000367053.5:c.786G>T	ENSP00000356020.1:p.Val262=
ENST00000400960.6:c.786G>T	ENSP00000383744.2:p.Val262=
ENST00000434033.5:n.713G>T
ENST00000436595.1:n.414+12255G>T
ENST00000450439.5:n.713G>T
ENST00000529814.1:c.713G>T
ENST00000534202.5:c.786G>T	ENSP00000436139.2:p.Val262=
NM_000573.3:c.786G>T	NP_000564.2:p.Val262=
NM_000651.4:c.786G>T	NP_000642.3:p.Val262=
XM_006711166.2:c.801G>T	XP_006711229.1:p.Val267=
XM_011509205.1:c.801G>T	XP_011507507.1:p.Val267=
NM_000651.5:c.786G>T	NP_000642.3:p.Val262=
XM_024453287.1:c.801G>T	XP_024309055.1:p.Val267=
NM_000573.4:c.786G>T	NP_000564.2:p.Val262=
NM_000651.6:c.786G>T MANE Select	NP_000642.3:p.Val262=