Canonical Allele Identifier: CA2483464786

Gene: CR1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207630807_207630824delinsTGATGACTCTATAAGTTA , CM000663.2:g.207630807_207630824delinsTGATGACTCTATAAGTTA	GRCh38
NC_000001.10:g.207804152_207804169delinsTGATGACTCTATAAGTTA , CM000663.1:g.207804152_207804169delinsTGATGACTCTATAAGTTA	GRCh37
NC_000001.9:g.205870775_205870792delinsTGATGACTCTATAAGTTA	NCBI36
NG_007481.1:g.139680_139697delinsTGATGACTCTATAAGTTA

Transcript Alleles

HGVS	Amino-acid change
ENST00000367049.9:c.7457+186_7457+203delinsTGATGACTCTATAAGTTA MANE Select	ENSP00000356016.4:n.7457+186_7457+203delinsTGATGACTCTATAAGTTA...
ENST00000367051.6:c.6107+186_6107+203delinsTGATGACTCTATAAGTTA	ENSP00000356018.1:n.6107+186_6107+203delinsTGATGACTCTATAAGTTA...
ENST00000367052.6:c.6107+186_6107+203delinsTGATGACTCTATAAGTTA	ENSP00000356019.1:n.6107+186_6107+203delinsTGATGACTCTATAAGTTA...
ENST00000367053.6:c.6107+186_6107+203delinsTGATGACTCTATAAGTTA	ENSP00000356020.1:n.6107+186_6107+203delinsTGATGACTCTATAAGTTA...
ENST00000400960.7:c.6107+186_6107+203delinsTGATGACTCTATAAGTTA	ENSP00000383744.2:n.6107+186_6107+203delinsTGATGACTCTATAAGTTA...
ENST00000367049.8:c.7457+186_7457+203delinsTGATGACTCTATAAGTTA	ENSP00000356016.4:n.7457+186_7457+203delinsTGATGACTCTATAAGTTA...
ENST00000367051.5:c.6107+186_6107+203delinsTGATGACTCTATAAGTTA	ENSP00000356018.1:n.6107+186_6107+203delinsTGATGACTCTATAAGTTA...
ENST00000367052.5:c.6107+186_6107+203delinsTGATGACTCTATAAGTTA	ENSP00000356019.1:n.6107+186_6107+203delinsTGATGACTCTATAAGTTA...
ENST00000367053.5:c.6107+186_6107+203delinsTGATGACTCTATAAGTTA	ENSP00000356020.1:n.6107+186_6107+203delinsTGATGACTCTATAAGTTA...
ENST00000400960.6:c.6107+186_6107+203delinsTGATGACTCTATAAGTTA	ENSP00000383744.2:n.6107+186_6107+203delinsTGATGACTCTATAAGTTA...
NM_000573.3:c.6107+186_6107+203delinsTGATGACTCTATAAGTTA	NP_000564.2:n.6107+186_6107+203delinsTGATGACTCTATAAGTTA
NM_000651.4:c.7457+186_7457+203delinsTGATGACTCTATAAGTTA	NP_000642.3:n.7457+186_7457+203delinsTGATGACTCTATAAGTTA
XM_006711166.2:c.7367+7739_7367+7756delinsTGATGACTCTATAAGTTA	XP_006711229.1:n.7367+7739_7367+7756delinsTGATGACTCTATAAGTTA
XM_011509205.1:c.7472+186_7472+203delinsTGATGACTCTATAAGTTA	XP_011507507.1:n.7472+186_7472+203delinsTGATGACTCTATAAGTTA
NM_000651.5:c.7457+186_7457+203delinsTGATGACTCTATAAGTTA	NP_000642.3:n.7457+186_7457+203delinsTGATGACTCTATAAGTTA
XM_024453287.1:c.6122+186_6122+203delinsTGATGACTCTATAAGTTA	XP_024309055.1:n.6122+186_6122+203delinsTGATGACTCTATAAGTTA
NM_000573.4:c.6107+186_6107+203delinsTGATGACTCTATAAGTTA	NP_000564.2:n.6107+186_6107+203delinsTGATGACTCTATAAGTTA
NM_000651.6:c.7457+186_7457+203delinsTGATGACTCTATAAGTTA MANE Select	NP_000642.3:n.7457+186_7457+203delinsTGATGACTCTATAAGTTA