Canonical Allele Identifier: CA2683748889

Gene: CALCR

Linked Data

• gnomAD v4: 7-93426482-C-CGCA

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93426488_93426490dup , CM000669.2:g.93426488_93426490dup	GRCh38
NC_000007.13:g.93055800_93055802dup , CM000669.1:g.93055800_93055802dup	GRCh37
NC_000007.12:g.92893736_92893738dup	NCBI36
NG_013005.1:g.153246_153248dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426151.7:c.1296_1298dup MANE Select	ENSP00000389295.1:p.Ala433_Glu434insAla
ENST00000649521.1:c.1344_1346dup	ENSP00000497687.1:p.Ala449_Glu450insAla
ENST00000359558.6:c.1398_1400dup	ENSP00000352561.2:p.Ala467_Glu468insAla
ENST00000360249.8:c.*806_*808dup	ENSP00000353385.5:n.*806_*808dup
ENST00000394441.5:c.1296_1298dup	ENSP00000377959.1:p.Ala433_Glu434insAla
ENST00000415529.2:c.1346_1348dup	ENSP00000413179.1:n.1346_1348dup
ENST00000421592.5:c.1344_1346dup	ENSP00000399552.1:p.Ala449_Glu450insAla
ENST00000423724.5:c.1394_1396dup	ENSP00000391369.1:n.1394_1396dup
ENST00000426151.5:c.1296_1298dup	ENSP00000389295.1:p.Ala433_Glu434insAla
NM_001164737.1:c.1398_1400dup	NP_001158209.1:p.Ala467_Glu468insAla
NM_001164738.1:c.1296_1298dup	NP_001158210.1:p.Ala433_Glu434insAla
NM_001742.3:c.1296_1298dup	NP_001733.1:p.Ala433_Glu434insAla
NM_001164737.2:c.1344_1346dup	NP_001158209.2:p.Ala449_Glu450insAla
NM_001742.4:c.1296_1298dup MANE Select	NP_001733.1:p.Ala433_Glu434insAla
NM_001164737.3:c.1344_1346dup	NP_001158209.2:p.Ala449_Glu450insAla
NM_001164738.2:c.1296_1298dup	NP_001158210.1:p.Ala433_Glu434insAla