Canonical Allele Identifier: CA2483433131

Gene: CR1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207523565C= , CM000663.2:g.207523565C=	GRCh38
NC_000001.10:g.207696910C= , CM000663.1:g.207696910C=	GRCh37
NC_000001.9:g.205763533C=	NCBI36
NG_007481.1:g.32438C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000367049.9:c.488-46C= MANE Select	ENSP00000356016.4:n.488-46C=
ENST00000367051.6:c.487+11911C=	ENSP00000356018.1:n.487+11911C=
ENST00000367052.6:c.488-46C=	ENSP00000356019.1:n.488-46C=
ENST00000367053.6:c.488-46C=	ENSP00000356020.1:n.488-46C=
ENST00000400960.7:c.488-46C=	ENSP00000383744.2:n.488-46C=
ENST00000367049.8:c.488-46C=	ENSP00000356016.4:n.488-46C=
ENST00000367050.8:n.609-46C=
ENST00000367051.5:c.487+11911C=	ENSP00000356018.1:n.487+11911C=
ENST00000367052.5:c.488-46C=	ENSP00000356019.1:n.488-46C=
ENST00000367053.5:c.488-46C=	ENSP00000356020.1:n.488-46C=
ENST00000400960.6:c.488-46C=	ENSP00000383744.2:n.488-46C=
ENST00000434033.5:n.415-46C=
ENST00000436595.1:n.414+11911C=
ENST00000450439.5:n.415-46C=
ENST00000529814.1:c.415-46C=
ENST00000534202.5:c.488-46C=	ENSP00000436139.2:n.488-46C=
NM_000573.3:c.488-46C=	NP_000564.2:n.488-46C=
NM_000651.4:c.488-46C=	NP_000642.3:n.488-46C=
XM_006711166.2:c.503-46C=	XP_006711229.1:n.503-46C=
XM_011509205.1:c.503-46C=	XP_011507507.1:n.503-46C=
NM_000651.5:c.488-46C=	NP_000642.3:n.488-46C=
XM_024453287.1:c.503-46C=	XP_024309055.1:n.503-46C=
NM_000573.4:c.488-46C=	NP_000564.2:n.488-46C=
NM_000651.6:c.488-46C= MANE Select	NP_000642.3:n.488-46C=