Canonical Allele Identifier: CA843978520

Gene: CALCR

Linked Data

• dbSNP Id: rs1181971499
• MyVariant Identifiers: chr7:g.93055813_93055814insGAGCA (hg19) ; chr7:g.93426501_93426502insGAGCA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93426506_93426510dup , CM000669.2:g.93426506_93426510dup	GRCh38
NC_000007.13:g.93055818_93055822dup , CM000669.1:g.93055818_93055822dup	GRCh37
NC_000007.12:g.92893754_92893758dup	NCBI36
NG_013005.1:g.153225_153229dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426151.7:c.1275_1279dup MANE Select	ENSP00000389295.1:p.Arg427LeufsTer23
ENST00000649521.1:c.1323_1327dup	ENSP00000497687.1:p.Arg443LeufsTer23
ENST00000359558.6:c.1377_1381dup	ENSP00000352561.2:p.Arg461LeufsTer23
ENST00000360249.8:c.*785_*789dup	ENSP00000353385.5:n.*785_*789dup
ENST00000394441.5:c.1275_1279dup	ENSP00000377959.1:p.Arg427LeufsTer23
ENST00000415529.2:c.1325_1329dup	ENSP00000413179.1:n.1325_1329dup
ENST00000421592.5:c.1323_1327dup	ENSP00000399552.1:p.Arg443LeufsTer23
ENST00000423724.5:c.1373_1377dup	ENSP00000391369.1:n.1373_1377dup
ENST00000426151.5:c.1275_1279dup	ENSP00000389295.1:p.Arg427LeufsTer23
NM_001164737.1:c.1377_1381dup	NP_001158209.1:p.Arg461LeufsTer23
NM_001164738.1:c.1275_1279dup	NP_001158210.1:p.Arg427LeufsTer23
NM_001742.3:c.1275_1279dup	NP_001733.1:p.Arg427LeufsTer23
NM_001164737.2:c.1323_1327dup	NP_001158209.2:p.Arg443LeufsTer23
NM_001742.4:c.1275_1279dup MANE Select	NP_001733.1:p.Arg427LeufsTer23
NM_001164737.3:c.1323_1327dup	NP_001158209.2:p.Arg443LeufsTer23
NM_001164738.2:c.1275_1279dup	NP_001158210.1:p.Arg427LeufsTer23