Canonical Allele Identifier: CA651749567

Gene: CALCR

Linked Data

• COSMIC: COSN8047257

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93426088T>G , CM000669.2:g.93426088T>G	GRCh38
NC_000007.13:g.93055400T>G , CM000669.1:g.93055400T>G	GRCh37
NC_000007.12:g.92893336T>G	NCBI36
NG_013005.1:g.153643A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426151.7:c.*268A>C MANE Select	ENSP00000389295.1:n.*268A>C
ENST00000649521.1:c.*268A>C	ENSP00000497687.1:n.*268A>C
ENST00000359558.6:c.*268A>C	ENSP00000352561.2:n.*268A>C
ENST00000421592.5:c.*268A>C	ENSP00000399552.1:n.*268A>C
NM_001164737.1:c.*268A>C	NP_001158209.1:n.*268A>C
NM_001164738.1:c.*268A>C	NP_001158210.1:n.*268A>C
NM_001742.3:c.*268A>C	NP_001733.1:n.*268A>C
NM_001164737.2:c.*268A>C	NP_001158209.2:n.*268A>C
NM_001742.4:c.*268A>C MANE Select	NP_001733.1:n.*268A>C
NM_001164737.3:c.*268A>C	NP_001158209.2:n.*268A>C
NM_001164738.2:c.*268A>C	NP_001158210.1:n.*268A>C