Canonical Allele Identifier: CA2483443621

Gene: CR1

Linked Data

• dbSNP Id: rs1660888668

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207580183del , CM000663.2:g.207580183del	GRCh38
NC_000001.10:g.207753528del , CM000663.1:g.207753528del	GRCh37
NC_000001.9:g.205820151del	NCBI36
NG_007481.1:g.89056del

Transcript Alleles

HGVS	Amino-acid change
ENST00000367049.9:c.4937-57del MANE Select	ENSP00000356016.4:n.4937-57del
ENST00000367051.6:c.3587-57del	ENSP00000356018.1:n.3587-57del
ENST00000367052.6:c.3587-57del	ENSP00000356019.1:n.3587-57del
ENST00000367053.6:c.3587-57del	ENSP00000356020.1:n.3587-57del
ENST00000400960.7:c.3587-57del	ENSP00000383744.2:n.3587-57del
ENST00000367049.8:c.4937-57del	ENSP00000356016.4:n.4937-57del
ENST00000367051.5:c.3587-57del	ENSP00000356018.1:n.3587-57del
ENST00000367052.5:c.3587-57del	ENSP00000356019.1:n.3587-57del
ENST00000367053.5:c.3587-57del	ENSP00000356020.1:n.3587-57del
ENST00000400960.6:c.3587-57del	ENSP00000383744.2:n.3587-57del
ENST00000529814.1:c.1179+14260del
ENST00000534202.5:c.*702-57del	ENSP00000436139.2:n.*702-57del
NM_000573.3:c.3587-57del	NP_000564.2:n.3587-57del
NM_000651.4:c.4937-57del	NP_000642.3:n.4937-57del
XM_006711166.2:c.4952-57del	XP_006711229.1:n.4952-57del
XM_011509205.1:c.4952-57del	XP_011507507.1:n.4952-57del
NM_000651.5:c.4937-57del	NP_000642.3:n.4937-57del
XM_024453287.1:c.3602-57del	XP_024309055.1:n.3602-57del
NM_000573.4:c.3587-57del	NP_000564.2:n.3587-57del
NM_000651.6:c.4937-57del MANE Select	NP_000642.3:n.4937-57del