Canonical Allele Identifier: CA2650269929

Gene: CR1

Linked Data

• gnomAD v4: 1-207611878-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207611880del , CM000663.2:g.207611880del	GRCh38
NC_000001.10:g.207785225del , CM000663.1:g.207785225del	GRCh37
NC_000001.9:g.205851848del	NCBI36
NG_007481.1:g.120753del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367049.9:c.6472+27del MANE Select	ENSP00000356016.4:n.6472+27del
ENST00000367051.6:c.5122+27del	ENSP00000356018.1:n.5122+27del
ENST00000367052.6:c.5122+27del	ENSP00000356019.1:n.5122+27del
ENST00000367053.6:c.5122+27del	ENSP00000356020.1:n.5122+27del
ENST00000400960.7:c.5122+27del	ENSP00000383744.2:n.5122+27del
ENST00000367049.8:c.6472+27del	ENSP00000356016.4:n.6472+27del
ENST00000367051.5:c.5122+27del	ENSP00000356018.1:n.5122+27del
ENST00000367052.5:c.5122+27del	ENSP00000356019.1:n.5122+27del
ENST00000367053.5:c.5122+27del	ENSP00000356020.1:n.5122+27del
ENST00000400960.6:c.5122+27del	ENSP00000383744.2:n.5122+27del
ENST00000529814.1:c.1180-4695del
NM_000573.3:c.5122+27del	NP_000564.2:n.5122+27del
NM_000651.4:c.6472+27del	NP_000642.3:n.6472+27del
XM_006711166.2:c.6487+27del	XP_006711229.1:n.6487+27del
XM_011509205.1:c.6487+27del	XP_011507507.1:n.6487+27del
NM_000651.5:c.6472+27del	NP_000642.3:n.6472+27del
XM_024453287.1:c.5137+27del	XP_024309055.1:n.5137+27del
NM_000573.4:c.5122+27del	NP_000564.2:n.5122+27del
NM_000651.6:c.6472+27del MANE Select	NP_000642.3:n.6472+27del