Canonical Allele Identifier: CA2650266348

Gene: CR1

Linked Data

• gnomAD v4: 1-207523573-AAACT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207523574_207523577del , CM000663.2:g.207523574_207523577del	GRCh38
NC_000001.10:g.207696919_207696922del , CM000663.1:g.207696919_207696922del	GRCh37
NC_000001.9:g.205763542_205763545del	NCBI36
NG_007481.1:g.32447_32450del

Transcript Alleles

HGVS	Amino-acid change
ENST00000367049.9:c.488-37_488-34del MANE Select	ENSP00000356016.4:n.488-37_488-34del
ENST00000367051.6:c.487+11920_487+11923del	ENSP00000356018.1:n.487+11920_487+11923del
ENST00000367052.6:c.488-37_488-34del	ENSP00000356019.1:n.488-37_488-34del
ENST00000367053.6:c.488-37_488-34del	ENSP00000356020.1:n.488-37_488-34del
ENST00000400960.7:c.488-37_488-34del	ENSP00000383744.2:n.488-37_488-34del
ENST00000367049.8:c.488-37_488-34del	ENSP00000356016.4:n.488-37_488-34del
ENST00000367050.8:n.609-37_609-34del
ENST00000367051.5:c.487+11920_487+11923del	ENSP00000356018.1:n.487+11920_487+11923del
ENST00000367052.5:c.488-37_488-34del	ENSP00000356019.1:n.488-37_488-34del
ENST00000367053.5:c.488-37_488-34del	ENSP00000356020.1:n.488-37_488-34del
ENST00000400960.6:c.488-37_488-34del	ENSP00000383744.2:n.488-37_488-34del
ENST00000434033.5:n.415-37_415-34del
ENST00000436595.1:n.414+11920_414+11923del
ENST00000450439.5:n.415-37_415-34del
ENST00000529814.1:c.415-37_415-34del
ENST00000534202.5:c.488-37_488-34del	ENSP00000436139.2:n.488-37_488-34del
NM_000573.3:c.488-37_488-34del	NP_000564.2:n.488-37_488-34del
NM_000651.4:c.488-37_488-34del	NP_000642.3:n.488-37_488-34del
XM_006711166.2:c.503-37_503-34del	XP_006711229.1:n.503-37_503-34del
XM_011509205.1:c.503-37_503-34del	XP_011507507.1:n.503-37_503-34del
NM_000651.5:c.488-37_488-34del	NP_000642.3:n.488-37_488-34del
XM_024453287.1:c.503-37_503-34del	XP_024309055.1:n.503-37_503-34del
NM_000573.4:c.488-37_488-34del	NP_000564.2:n.488-37_488-34del
NM_000651.6:c.488-37_488-34del MANE Select	NP_000642.3:n.488-37_488-34del