Canonical Allele Identifier: CA3047154509

Gene: CR1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207609585_207609586delinsTG , CM000663.2:g.207609585_207609586delinsTG	GRCh38
NC_000001.10:g.207782930_207782931delinsTG , CM000663.1:g.207782930_207782931delinsTG	GRCh37
NC_000001.9:g.205849553_205849554delinsTG	NCBI36
NG_007481.1:g.118458_118459delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367049.9:c.6192_6193delinsTG MANE Select	ENSP00000356016.4:p.Ile2065Val
ENST00000367051.6:c.4842_4843delinsTG	ENSP00000356018.1:p.Ile1615Val
ENST00000367052.6:c.4842_4843delinsTG	ENSP00000356019.1:p.Ile1615Val
ENST00000367053.6:c.4842_4843delinsTG	ENSP00000356020.1:p.Ile1615Val
ENST00000400960.7:c.4842_4843delinsTG	ENSP00000383744.2:p.Ile1615Val
ENST00000367049.8:c.6192_6193delinsTG	ENSP00000356016.4:p.Ile2065Val
ENST00000367051.5:c.4842_4843delinsTG	ENSP00000356018.1:p.Ile1615Val
ENST00000367052.5:c.4842_4843delinsTG	ENSP00000356019.1:p.Ile1615Val
ENST00000367053.5:c.4842_4843delinsTG	ENSP00000356020.1:p.Ile1615Val
ENST00000400960.6:c.4842_4843delinsTG	ENSP00000383744.2:p.Ile1615Val
ENST00000529814.1:c.1180-6990_1180-6989delinsTG
NM_000573.3:c.4842_4843delinsTG	NP_000564.2:p.Ile1615Val
NM_000651.4:c.6192_6193delinsTG	NP_000642.3:p.Ile2065Val
XM_006711166.2:c.6207_6208delinsTG	XP_006711229.1:p.Ile2070Val
XM_011509205.1:c.6207_6208delinsTG	XP_011507507.1:p.Ile2070Val
NM_000651.5:c.6192_6193delinsTG	NP_000642.3:p.Ile2065Val
XM_024453287.1:c.4857_4858delinsTG	XP_024309055.1:p.Ile1620Val
NM_000573.4:c.4842_4843delinsTG	NP_000564.2:p.Ile1615Val
NM_000651.6:c.6192_6193delinsTG MANE Select	NP_000642.3:p.Ile2065Val