Canonical Allele Identifier: CA651749566

Gene: CALCR

Linked Data

• COSMIC: COSN21628439

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93426030_93426031insC , CM000669.2:g.93426030_93426031insC	GRCh38
NC_000007.13:g.93055342_93055343insC , CM000669.1:g.93055342_93055343insC	GRCh37
NC_000007.12:g.92893278_92893279insC	NCBI36
NG_013005.1:g.153700_153701insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426151.7:c.*325_*326insG MANE Select	ENSP00000389295.1:n.*325_*326insG
ENST00000649521.1:c.*325_*326insG	ENSP00000497687.1:n.*325_*326insG
ENST00000359558.6:c.*325_*326insG	ENSP00000352561.2:n.*325_*326insG
ENST00000421592.5:c.*325_*326insG	ENSP00000399552.1:n.*325_*326insG
NM_001164737.1:c.*325_*326insG	NP_001158209.1:n.*325_*326insG
NM_001164738.1:c.*325_*326insG	NP_001158210.1:n.*325_*326insG
NM_001742.3:c.*325_*326insG	NP_001733.1:n.*325_*326insG
NM_001164737.2:c.*325_*326insG	NP_001158209.2:n.*325_*326insG
NM_001742.4:c.*325_*326insG MANE Select	NP_001733.1:n.*325_*326insG
NM_001164737.3:c.*325_*326insG	NP_001158209.2:n.*325_*326insG
NM_001164738.2:c.*325_*326insG	NP_001158210.1:n.*325_*326insG