Canonical Allele Identifier: CA2650269836

Gene: CR1

Linked Data

• gnomAD v4: 1-207611527-GTT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207611528_207611529del , CM000663.2:g.207611528_207611529del	GRCh38
NC_000001.10:g.207784873_207784874del , CM000663.1:g.207784873_207784874del	GRCh37
NC_000001.9:g.205851496_205851497del	NCBI36
NG_007481.1:g.120401_120402del

Transcript Alleles

HGVS	Amino-acid change
ENST00000367049.9:c.6296-149_6296-148del MANE Select	ENSP00000356016.4:n.6296-149_6296-148del
ENST00000367051.6:c.4946-149_4946-148del	ENSP00000356018.1:n.4946-149_4946-148del
ENST00000367052.6:c.4946-149_4946-148del	ENSP00000356019.1:n.4946-149_4946-148del
ENST00000367053.6:c.4946-149_4946-148del	ENSP00000356020.1:n.4946-149_4946-148del
ENST00000400960.7:c.4946-149_4946-148del	ENSP00000383744.2:n.4946-149_4946-148del
ENST00000367049.8:c.6296-149_6296-148del	ENSP00000356016.4:n.6296-149_6296-148del
ENST00000367051.5:c.4946-149_4946-148del	ENSP00000356018.1:n.4946-149_4946-148del
ENST00000367052.5:c.4946-149_4946-148del	ENSP00000356019.1:n.4946-149_4946-148del
ENST00000367053.5:c.4946-149_4946-148del	ENSP00000356020.1:n.4946-149_4946-148del
ENST00000400960.6:c.4946-149_4946-148del	ENSP00000383744.2:n.4946-149_4946-148del
ENST00000529814.1:c.1180-5047_1180-5046del
NM_000573.3:c.4946-149_4946-148del	NP_000564.2:n.4946-149_4946-148del
NM_000651.4:c.6296-149_6296-148del	NP_000642.3:n.6296-149_6296-148del
XM_006711166.2:c.6311-149_6311-148del	XP_006711229.1:n.6311-149_6311-148del
XM_011509205.1:c.6311-149_6311-148del	XP_011507507.1:n.6311-149_6311-148del
NM_000651.5:c.6296-149_6296-148del	NP_000642.3:n.6296-149_6296-148del
XM_024453287.1:c.4961-149_4961-148del	XP_024309055.1:n.4961-149_4961-148del
NM_000573.4:c.4946-149_4946-148del	NP_000564.2:n.4946-149_4946-148del
NM_000651.6:c.6296-149_6296-148del MANE Select	NP_000642.3:n.6296-149_6296-148del