Canonical Allele Identifier: CA1726312490

Gene: CALCR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93426488_93426491delinsAGCG , CM000669.2:g.93426488_93426491delinsAGCG	GRCh38
NC_000007.13:g.93055800_93055803delinsAGCG , CM000669.1:g.93055800_93055803delinsAGCG	GRCh37
NC_000007.12:g.92893736_92893739delinsAGCG	NCBI36
NG_013005.1:g.153240_153243delinsCGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426151.7:c.1290_1293delinsCGCT MANE Select	ENSP00000389295.1:p.Ala430=
ENST00000649521.1:c.1338_1341delinsCGCT	ENSP00000497687.1:p.Ala446=
ENST00000359558.6:c.1392_1395delinsCGCT	ENSP00000352561.2:p.Ala464=
ENST00000360249.8:c.*800_*803delinsCGCT	ENSP00000353385.5:n.*800_*803delinsCGCT
ENST00000394441.5:c.1290_1293delinsCGCT	ENSP00000377959.1:p.Ala430=
ENST00000415529.2:c.1340_1343delinsCGCT	ENSP00000413179.1:n.1340_1343delinsCGCT
ENST00000421592.5:c.1338_1341delinsCGCT	ENSP00000399552.1:p.Ala446=
ENST00000423724.5:c.1388_1391delinsCGCT	ENSP00000391369.1:n.1388_1391delinsCGCT
ENST00000426151.5:c.1290_1293delinsCGCT	ENSP00000389295.1:p.Ala430=
NM_001164737.1:c.1392_1395delinsCGCT	NP_001158209.1:p.Ala464=
NM_001164738.1:c.1290_1293delinsCGCT	NP_001158210.1:p.Ala430=
NM_001742.3:c.1290_1293delinsCGCT	NP_001733.1:p.Ala430=
NM_001164737.2:c.1338_1341delinsCGCT	NP_001158209.2:p.Ala446=
NM_001742.4:c.1290_1293delinsCGCT MANE Select	NP_001733.1:p.Ala430=
NM_001164737.3:c.1338_1341delinsCGCT	NP_001158209.2:p.Ala446=
NM_001164738.2:c.1290_1293delinsCGCT	NP_001158210.1:p.Ala430=