Canonical Allele Identifier: CA1139928092

Gene: CR1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207621975A= , CM000663.2:g.207621975A=	GRCh38
NC_000001.10:g.207795320A= , CM000663.1:g.207795320A=	GRCh37
NC_000001.9:g.205861943A=	NCBI36
NG_007481.1:g.130848A=

Transcript Alleles

HGVS	Amino-acid Change
NM_000651.6:c.7255A= MANE Select	NP_000642.3:p.Thr2419=
ENST00000367049.9:c.7255A= MANE Select	ENSP00000356016.4:p.Thr2419=
NM_000573.3:c.5905A=	NP_000564.2:p.Thr1969=
NM_000573.4:c.5905A=	NP_000564.2:p.Thr1969=
NM_000651.4:c.7255A=	NP_000642.3:p.Thr2419=
NM_000651.5:c.7255A=	NP_000642.3:p.Thr2419=
ENST00000367049.8:c.7255A=	ENSP00000356016.4:p.Thr2419=
ENST00000367051.5:c.5905A=	ENSP00000356018.1:p.Thr1969=
ENST00000367051.6:c.5905A=	ENSP00000356018.1:p.Thr1969=
ENST00000367052.5:c.5905A=	ENSP00000356019.1:p.Thr1969=
ENST00000367052.6:c.5905A=	ENSP00000356019.1:p.Thr1969=
ENST00000367053.5:c.5905A=	ENSP00000356020.1:p.Thr1969=
ENST00000367053.6:c.5905A=	ENSP00000356020.1:p.Thr1969=
ENST00000400960.6:c.5905A=	ENSP00000383744.2:p.Thr1969=
ENST00000400960.7:c.5905A=	ENSP00000383744.2:p.Thr1969=
ENST00000529814.1:c.1773A=
XM_006711166.2:c.7270A=	XP_006711229.1:p.Thr2424=
XM_011509205.1:c.7270A=	XP_011507507.1:p.Thr2424=
XM_024453287.1:c.5920A=	XP_024309055.1:p.Thr1974=