Canonical Allele Identifier: CA162017826

Gene: CALCR

Linked Data

• dbSNP Id: rs772403080
• MyVariant Identifiers: chr7:g.93055653_93055654insTGTT (hg19) ; chr7:g.93426341_93426342insTGTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93426344_93426347dup , CM000669.2:g.93426344_93426347dup	GRCh38
NC_000007.13:g.93055656_93055659dup , CM000669.1:g.93055656_93055659dup	GRCh37
NC_000007.12:g.92893592_92893595dup	NCBI36
NG_013005.1:g.153386_153389dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000426151.7:c.*11_*14dup MANE Select	ENSP00000389295.1:n.*11_*14dup
ENST00000649521.1:c.*11_*14dup	ENSP00000497687.1:n.*11_*14dup
ENST00000359558.6:c.*11_*14dup	ENSP00000352561.2:n.*11_*14dup
ENST00000360249.8:c.*946_*949dup	ENSP00000353385.5:n.*946_*949dup
ENST00000394441.5:c.*11_*14dup	ENSP00000377959.1:n.*11_*14dup
ENST00000421592.5:c.*11_*14dup	ENSP00000399552.1:n.*11_*14dup
ENST00000426151.5:c.*11_*14dup	ENSP00000389295.1:n.*11_*14dup
NM_001164737.1:c.*11_*14dup	NP_001158209.1:n.*11_*14dup
NM_001164738.1:c.*11_*14dup	NP_001158210.1:n.*11_*14dup
NM_001742.3:c.*11_*14dup	NP_001733.1:n.*11_*14dup
NM_001164737.2:c.*11_*14dup	NP_001158209.2:n.*11_*14dup
NM_001742.4:c.*11_*14dup MANE Select	NP_001733.1:n.*11_*14dup
NM_001164737.3:c.*11_*14dup	NP_001158209.2:n.*11_*14dup
NM_001164738.2:c.*11_*14dup	NP_001158210.1:n.*11_*14dup