Canonical Allele Identifier: CA651749568

Gene: CALCR

Linked Data

• COSMIC: COSN16263213

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93426176_93426177insC , CM000669.2:g.93426176_93426177insC	GRCh38
NC_000007.13:g.93055488_93055489insC , CM000669.1:g.93055488_93055489insC	GRCh37
NC_000007.12:g.92893424_92893425insC	NCBI36
NG_013005.1:g.153554_153555insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426151.7:c.*179_*180insG MANE Select	ENSP00000389295.1:n.*179_*180insG
ENST00000649521.1:c.*179_*180insG	ENSP00000497687.1:n.*179_*180insG
ENST00000359558.6:c.*179_*180insG	ENSP00000352561.2:n.*179_*180insG
ENST00000421592.5:c.*179_*180insG	ENSP00000399552.1:n.*179_*180insG
NM_001164737.1:c.*179_*180insG	NP_001158209.1:n.*179_*180insG
NM_001164738.1:c.*179_*180insG	NP_001158210.1:n.*179_*180insG
NM_001742.3:c.*179_*180insG	NP_001733.1:n.*179_*180insG
NM_001164737.2:c.*179_*180insG	NP_001158209.2:n.*179_*180insG
NM_001742.4:c.*179_*180insG MANE Select	NP_001733.1:n.*179_*180insG
NM_001164737.3:c.*179_*180insG	NP_001158209.2:n.*179_*180insG
NM_001164738.2:c.*179_*180insG	NP_001158210.1:n.*179_*180insG