Canonical Allele Identifier: CA1726312313

Gene: CALCR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93426073_93426074delinsGT , CM000669.2:g.93426073_93426074delinsGT	GRCh38
NC_000007.13:g.93055385_93055386delinsGT , CM000669.1:g.93055385_93055386delinsGT	GRCh37
NC_000007.12:g.92893321_92893322delinsGT	NCBI36
NG_013005.1:g.153657_153658delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426151.7:c.*282_*283delinsAC MANE Select	ENSP00000389295.1:n.*282_*283delinsAC
ENST00000649521.1:c.*282_*283delinsAC	ENSP00000497687.1:n.*282_*283delinsAC
ENST00000359558.6:c.*282_*283delinsAC	ENSP00000352561.2:n.*282_*283delinsAC
ENST00000421592.5:c.*282_*283delinsAC	ENSP00000399552.1:n.*282_*283delinsAC
NM_001164737.1:c.*282_*283delinsAC	NP_001158209.1:n.*282_*283delinsAC
NM_001164738.1:c.*282_*283delinsAC	NP_001158210.1:n.*282_*283delinsAC
NM_001742.3:c.*282_*283delinsAC	NP_001733.1:n.*282_*283delinsAC
NM_001164737.2:c.*282_*283delinsAC	NP_001158209.2:n.*282_*283delinsAC
NM_001742.4:c.*282_*283delinsAC MANE Select	NP_001733.1:n.*282_*283delinsAC
NM_001164737.3:c.*282_*283delinsAC	NP_001158209.2:n.*282_*283delinsAC
NM_001164738.2:c.*282_*283delinsAC	NP_001158210.1:n.*282_*283delinsAC