Canonical Allele Identifier: CA2483456531

Gene: CR1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207611715_207611716delinsAC , CM000663.2:g.207611715_207611716delinsAC	GRCh38
NC_000001.10:g.207785060_207785061delinsAC , CM000663.1:g.207785060_207785061delinsAC	GRCh37
NC_000001.9:g.205851683_205851684delinsAC	NCBI36
NG_007481.1:g.120588_120589delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367049.9:c.6334_6335delinsAC MANE Select	ENSP00000356016.4:p.Thr2112=
ENST00000367051.6:c.4984_4985delinsAC	ENSP00000356018.1:p.Thr1662=
ENST00000367052.6:c.4984_4985delinsAC	ENSP00000356019.1:p.Thr1662=
ENST00000367053.6:c.4984_4985delinsAC	ENSP00000356020.1:p.Thr1662=
ENST00000400960.7:c.4984_4985delinsAC	ENSP00000383744.2:p.Thr1662=
ENST00000367049.8:c.6334_6335delinsAC	ENSP00000356016.4:p.Thr2112=
ENST00000367051.5:c.4984_4985delinsAC	ENSP00000356018.1:p.Thr1662=
ENST00000367052.5:c.4984_4985delinsAC	ENSP00000356019.1:p.Thr1662=
ENST00000367053.5:c.4984_4985delinsAC	ENSP00000356020.1:p.Thr1662=
ENST00000400960.6:c.4984_4985delinsAC	ENSP00000383744.2:p.Thr1662=
ENST00000529814.1:c.1180-4860_1180-4859delinsAC
NM_000573.3:c.4984_4985delinsAC	NP_000564.2:p.Thr1662=
NM_000651.4:c.6334_6335delinsAC	NP_000642.3:p.Thr2112=
XM_006711166.2:c.6349_6350delinsAC	XP_006711229.1:p.Thr2117=
XM_011509205.1:c.6349_6350delinsAC	XP_011507507.1:p.Thr2117=
NM_000651.5:c.6334_6335delinsAC	NP_000642.3:p.Thr2112=
XM_024453287.1:c.4999_5000delinsAC	XP_024309055.1:p.Thr1667=
NM_000573.4:c.4984_4985delinsAC	NP_000564.2:p.Thr1662=
NM_000651.6:c.6334_6335delinsAC MANE Select	NP_000642.3:p.Thr2112=